Original source

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

Alleles
G/T | Ancestral: G | Ambiguity code: K | MAF: 0.04 (T)
Location

Chromosome 1:26694624 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

1:g.26694624G>T

About this variant

This variant overlaps 3 transcripts and has 2506 individual genotypes.

Variation displays