LOC105376219

uncharacterized LOC105376219

Known Variants27 total

rsid	Position (GRCh37)	Alleles	Class	ClinVar
rs10980770	9:113,874,885	G/A	intergenic variant	—
rs374011220	9:113,878,924	G/C	—	—
rs369080900	9:113,888,018	G/A	—	—
rs144057735	9:113,889,738	G/A	intergenic variant	—
rs56038804	9:113,892,634	G/C	intergenic variant	—
rs28688399	9:113,896,438	T/A	intergenic variant	—
rs60698178	9:113,897,770	T/C	—	—
rs12339013	9:113,912,560	T/G	intron variant	—
rs10980799	9:113,915,529	T/C	intron variant	—
rs10980800	9:113,915,905	T/C	intron variant	—
rs7034139	9:113,924,517	C/A	intron variant	—
rs7023923	9:113,925,534	T/C	intron variant	—
rs12344280	9:113,925,642	G/A	intron variant	—
rs62569723	9:113,936,919	A/T	—	—
rs17812273	9:113,940,717	T/C	regulatory region variant	—
rs10123393	9:113,941,670	T/C	intron variant	—
rs115162333	9:113,945,620	T/G	—	—
rs28430334	9:113,950,883	A/G	intron variant	—
rs17207270	9:113,951,044	G/A	intron variant	—
rs190618272	9:113,954,891	C/T	intron variant	—
rs12345486	9:113,967,410	G/A	intron variant	—
rs143302730	9:113,985,535	T/G	intron variant	—
rs12685977	9:113,998,915	A/G	regulatory region variant	—
rs10114900	9:114,002,855	A/G	intron variant	—
rs62571883	9:114,012,572	G/C	intron variant	—
rs759787175	9:114,023,866	G/C	—	—
rs574633220	9:114,044,999	A/T	—	—

Gene information from NCBI Gene. Variant classifications from ClinVar.