Original source

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

Alleles
T/C | Ancestral: T | Ambiguity code: Y | MAF: 0.02 (C)
Location

Chromosome 10:111076155 (forward strand) | View in location tab

Most severe consequence
HGVS name

10:g.111076155T>C

About this variant

This variant overlaps 2 transcripts and has 2504 individual genotypes.

Variation displays