Original source

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

Alleles
G/A | Ancestral: A | Ambiguity code: R | MAF: 0.40 (G)
Location

Chromosome 16:57541163 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs57492751

HGVS name

16:g.57541163G>A

About this variant

This variant overlaps 8 transcripts and has 2583 individual genotypes.

Variation displays