Original source

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

Alleles
A/T | Ancestral: A | Ambiguity code: W | MAF: 0.08 (T)
Location

Chromosome 18:77248429 (forward strand) | View in location tab

Most severe consequence
HGVS name

18:g.77248429A>T

About this variant

This variant overlaps 1 transcript and has 2504 individual genotypes.

Variation displays