Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|View in dbSNP

Alleles
T/C|Ancestral: C|Ambiguity code: Y|MAF: 0.04 (C)
Location

Chromosome 10:23191641 (forward strand)|View in location tab

Most severe consequence
 
Upstream gene variant
Evidence status

HGVS name

10:g.23191641T>C

About this variant

This variant overlaps 1 transcript and has 2505 sample genotypes.

Variant displays