Original source

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

Alleles
T/A | Ancestral: T | Ambiguity code: W | MAF: 0.01 (A)
Location

Chromosome 2:192748338 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

2:g.192748338T>A

About this variant

This variant overlaps 2 transcripts and has 2504 individual genotypes.

Variation displays