Original source

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

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

Chromosome 5:161845762 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

5:g.161845762T>A

About this variant

This variant overlaps 7 transcripts and has 2504 individual genotypes.

Variation displays