DIRC3

disrupted in renal carcinoma 3

Known Variants34 total

rsid	Position (GRCh37)	Alleles	Class	ClinVar
rs9636273	2:218,239,814	A/G	—	—
rs10198955	2:218,244,298	C/A	—	—
rs6706673	2:218,251,702	G/C	—	—
rs6759952	2:218,271,719	T/A	—	—
rs1351164	2:218,271,898	T/G	—	—
rs1478575	2:218,278,555	T/A	intron variant	—
rs13395110	2:218,283,303	T/G	intron variant	—
rs994532	2:218,284,210	A/C	—	—
rs994533	2:218,284,278	G/C	intron variant	—
rs2373061	2:218,289,247	G/T	intron variant	—
rs10804260	2:218,290,048	C/T	coding sequence variant	—
rs11693806	2:218,292,158	C/T	coding sequence variant	—
rs57481445	2:218,296,374	A/G	intron variant	—
rs16857609	2:218,296,508	C/T	intron variant	—
rs16857611	2:218,296,732	C/T	intron variant	—
rs10084346	2:218,306,736	C/T	intron variant	—
rs966423	2:218,310,340	C/T	intron variant	—
rs11689435	2:218,314,253	C/T	intron variant	—
rs201030469	2:218,321,984	A/C	—	—
rs2373063	2:218,322,277	C/T	intron variant	—
rs9989823	2:218,371,201	C/T	intron variant	—
rs7579468	2:218,393,389	G/A	intron variant	—
rs139264983	2:218,400,902	T/C	intron variant	—
rs2568193	2:218,477,714	T/C	intron variant	—
rs2568187	2:218,482,187	A/C	—	—
rs150160188	2:218,484,881	A/T	intron variant	—
rs2052929	2:218,506,653	C/T	intron variant	—
rs6737145	2:218,513,292	A/G	intron variant	—
rs34183224	2:218,514,964	G/A	regulatory region variant	—
rs6435999	2:218,523,162	A/G	intron variant	—
rs62175364	2:218,530,679	G/A	intron variant	—
rs529892601	2:218,577,691	C/T	—	—
rs4672846	2:218,598,734	C/T	—	—
rs62182131	2:218,601,711	G/A	intron variant	—

Gene information from NCBI Gene. Variant classifications from ClinVar.