HEMGN

hemogen

Summary

Predicted to be involved in regulation of osteoblast differentiation. Located in nucleoplasm. [provided by Alliance of Genome Resources, Jul 2025]

Known Variants32 total

rsid	Position (GRCh37)	Alleles	Class	ClinVar
rs1304408669	9:100,689,733	G/C	—	uncertain significance
rs200368619	9:100,692,325	A/G	—	uncertain significance
rs1377398636	9:100,692,326	A/G	—	uncertain significance
rs35223978	9:100,692,330	G/A	—	benign
rs150117068	9:100,692,445	T/C	—	uncertain significance
rs1471564117	9:100,692,523	T/C	—	uncertain significance
rs138552503	9:100,692,563	G/T	—	uncertain significance
rs1269004076	9:100,692,568	G/A	—	uncertain significance
rs1372518143	9:100,692,596	G/T	—	uncertain significance
rs35527067	9:100,692,648	T/G	—	benign
rs752376629	9:100,692,668	C/T	—	uncertain significance
rs774870923	9:100,692,727	T/G	—	uncertain significance
rs1482895623	9:100,692,731	G/C	—	uncertain significance
rs753549435	9:100,692,774	T/C	—	uncertain significance
rs896163783	9:100,692,822	A/C	—	uncertain significance
rs140700506	9:100,692,841	G/T	—	uncertain significance
rs976201261	9:100,693,038	G/C	—	uncertain significance
rs191644480	9:100,693,118	A/G	—	likely benign
rs2490149684	9:100,693,156	G/T	—	uncertain significance
rs111240053	9:100,693,277	A/G	—	uncertain significance
rs1826939566	9:100,693,285	T/G	—	uncertain significance
rs777381979	9:100,693,306	G/A	—	uncertain significance
rs139664531	9:100,693,345	G/C	—	uncertain significance
rs759349655	9:100,693,373	C/T	—	uncertain significance
rs771744071	9:100,693,454	C/A	—	uncertain significance
rs767265129	9:100,693,460	G/C	—	uncertain significance
rs17431934	9:100,695,776	T/C	intron variant	—
rs755109	9:100,696,203	T/C	intron variant	—
rs7870723	9:100,699,242	T/C	intron variant	—
rs202223659	9:100,700,409	C/T	—	uncertain significance
rs3758253	9:100,700,654	C/G	—	—
rs10984466	9:100,707,992	A/G	upstream gene variant	—

Gene information from NCBI Gene. Variant classifications from ClinVar.