Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|View in dbSNP

Alleles
T/A|Ancestral: T|Ambiguity code: W|MAF: 0.03 (T)
Location

Chromosome 16:46682524 (forward strand)|View in location tab

Most severe consequence
 
3 prime UTR variant
Evidence status

Synonyms

Archive dbSNP rs58762896

HGVS names

This variant has 7 HGVS names - Show

About this variant

This variant overlaps 10 transcripts and has 2778 sample genotypes.

Variant displays