FOXH1
forkhead box H1
Summary
FOXH1 encodes a human homolog of Xenopus forkhead activin signal transducer-1. FOXH1 protein binds SMAD2 and activates an activin response element via binding the DNA motif TGT(G/T)(T/G)ATT. [provided by RefSeq, Jul 2008]
Known Variants199 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs576710211 | 8:145,699,149 | C/A | — | benign |
| rs886062751 | 8:145,699,170 | G/A | — | uncertain significance |
| rs1825046297 | 8:145,699,185 | C/T | — | uncertain significance |
| rs1825046517 | 8:145,699,191 | C/T | — | uncertain significance |
| rs1362803083 | 8:145,699,198 | C/T | — | uncertain significance |
| rs961808166 | 8:145,699,239 | G/A | — | uncertain significance |
| rs1825050087 | 8:145,699,267 | G/A | — | uncertain significance |
| rs1440626432 | 8:145,699,299 | G/T | — | uncertain significance |
| rs74360910 | 8:145,699,310 | G/A | — | benign |
| rs11781640 | 8:145,699,388 | C/T | — | likely benign |
| rs148389554 | 8:145,699,449 | G/C | — | uncertain significance |
| rs1024459830 | 8:145,699,533 | T/C | — | uncertain significance |
| rs562738425 | 8:145,699,547 | C/T | — | uncertain significance |
| rs192907579 | 8:145,699,566 | G/A | — | benign |
| rs541830947 | 8:145,699,598 | G/A | — | likely benign |
| rs1825066619 | 8:145,699,600 | G/T | — | uncertain significance |
| rs2721176 | 8:145,699,601 | T/C | — | benign |
| rs7833404 | 8:145,699,642 | C/T | — | benign |
| rs138782042 | 8:145,699,648 | G/A | — | likely benign |
| rs2537637404 | 8:145,699,659 | G/A | — | uncertain significance |
| rs770343068 | 8:145,699,662 | C/T | — | uncertain significance |
| rs142762918 | 8:145,699,663 | C/T | — | likely benign |
| rs762489738 | 8:145,699,664 | G/A | — | uncertain significance |
| rs150201264 | 8:145,699,669 | G/A | — | likely benign |
| rs138792321 | 8:145,699,670 | T/C | — | uncertain significance |
| rs1057522833 | 8:145,699,686 | C/T | — | uncertain significance |
| rs923325138 | 8:145,699,692 | C/T | — | uncertain significance |
| rs756111208 | 8:145,699,693 | G/A | — | likely benign |
| rs536501327 | 8:145,699,695 | C/T | — | uncertain significance |
| rs149382395 | 8:145,699,696 | G/A | — | likely benign |
| rs1421316442 | 8:145,699,715 | G/A | — | uncertain significance |
| rs2537637680 | 8:145,699,725 | G/A | — | uncertain significance |
| rs117754060 | 8:145,699,735 | G/C | — | likely benign |
| rs746265996 | 8:145,699,743 | C/G | — | uncertain significance |
| rs770253235 | 8:145,699,745 | C/T | — | uncertain significance |
| rs199639592 | 8:145,699,754 | C/A | — | uncertain significance |
| rs761520666 | 8:145,699,761 | G/A | — | uncertain significance |
| rs753781123 | 8:145,699,783 | C/T | — | likely benign |
| rs140090667 | 8:145,699,786 | C/G | — | uncertain significance |
| rs375647894 | 8:145,699,787 | C/T | — | uncertain significance |
| rs781308579 | 8:145,699,796 | G/A | — | uncertain significance |
| rs973088716 | 8:145,699,803 | T/C | — | uncertain significance |
| rs141411287 | 8:145,699,807 | C/A | — | likely benign |
| rs541715607 | 8:145,699,809 | G/C | — | uncertain significance |
| rs201165974 | 8:145,699,818 | G/A | — | uncertain significance |
| rs1341732331 | 8:145,699,830 | G/A | — | uncertain significance |
| rs2130035536 | 8:145,699,841 | A/C | — | uncertain significance |
| rs759544271 | 8:145,699,851 | C/T | — | uncertain significance |
| rs1237183304 | 8:145,699,852 | C/T | — | likely benign |
| rs765146615 | 8:145,699,855 | A/G | — | likely benign |
| rs767657157 | 8:145,699,860 | G/A | — | uncertain significance |
| rs949126117 | 8:145,699,863 | T/G | — | uncertain significance |
| rs201690019 | 8:145,699,876 | G/A | — | likely benign |
| rs1357197339 | 8:145,699,894 | C/T | — | likely benign |
| rs372121961 | 8:145,699,907 | G/A | — | uncertain significance |
| rs1011769775 | 8:145,699,910 | C/G | — | uncertain significance |
| rs934839135 | 8:145,699,916 | C/A | — | uncertain significance |
| rs759442283 | 8:145,699,924 | G/A | — | likely benign |
| rs769660425 | 8:145,699,925 | G/T | — | uncertain significance |
| rs775241333 | 8:145,699,928 | C/G | — | uncertain significance |
| rs886062752 | 8:145,699,934 | C/A | — | uncertain significance |
| rs151147114 | 8:145,699,936 | A/G | — | likely benign |
| rs760870582 | 8:145,699,939 | A/C | — | likely benign |
| rs1825079949 | 8:145,699,943 | G/A | — | uncertain significance |
| rs115750264 | 8:145,699,948 | G/A | — | benign |
| rs1825081652 | 8:145,699,956 | G/A | — | likely benign |
| rs1564751833 | 8:145,699,973 | G/A | — | uncertain significance |
| rs768693604 | 8:145,699,992 | G/A | — | uncertain significance |
| rs760782228 | 8:145,699,993 | G/A | — | likely benign |
| rs1239788503 | 8:145,699,999 | G/A | — | likely benign |
| rs372267255 | 8:145,700,005 | G/A | — | likely benign |
| rs1564751892 | 8:145,700,012 | C/T | — | uncertain significance |
| rs376840587 | 8:145,700,015 | C/T | — | uncertain significance |
| rs745445336 | 8:145,700,025 | T/C | — | uncertain significance |
| rs749154097 | 8:145,700,034 | C/T | — | uncertain significance |
| rs1205177041 | 8:145,700,039 | C/T | — | uncertain significance |
| rs1192153245 | 8:145,700,057 | G/C | — | uncertain significance |
| rs1392198480 | 8:145,700,059 | G/A | — | likely benign |
| rs770944195 | 8:145,700,066 | G/A | — | uncertain significance |
| rs2537639086 | 8:145,700,067 | G/A | — | uncertain significance |
| rs886044609 | 8:145,700,098 | T/G | — | uncertain significance |
| rs775697350 | 8:145,700,099 | G/A | — | uncertain significance |
| rs1224423317 | 8:145,700,100 | G/A | — | uncertain significance |
| rs763416777 | 8:145,700,102 | G/A | — | benign |
| rs1278245836 | 8:145,700,109 | C/A | — | uncertain significance |
| rs757842328 | 8:145,700,110 | C/T | — | likely benign |
| rs201853328 | 8:145,700,113 | C/T | — | likely benign |
| rs982305078 | 8:145,700,114 | T/G | — | uncertain significance |
| rs1460876038 | 8:145,700,120 | C/T | — | uncertain significance |
| rs748921328 | 8:145,700,135 | C/A | — | uncertain significance |
| rs778695747 | 8:145,700,142 | G/T | — | uncertain significance |
| rs1270394786 | 8:145,700,147 | G/A | — | uncertain significance |
| rs1192029881 | 8:145,700,152 | G/T | — | uncertain significance |
| rs570979595 | 8:145,700,158 | T/C | — | likely benign |
| rs371197993 | 8:145,700,159 | G/A | — | uncertain significance |
| rs763280219 | 8:145,700,162 | G/A | — | uncertain significance |
| rs200095132 | 8:145,700,171 | G/A | — | uncertain significance |
| rs752547489 | 8:145,700,190 | C/T | — | uncertain significance |
| rs758309990 | 8:145,700,192 | G/T | — | uncertain significance |
| rs374775293 | 8:145,700,194 | C/T | — | benign |
Showing 100 of 199 variants. Use the SNP search for the full list.
Gene information from NCBI Gene. Variant classifications from ClinVar.