Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | 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