Original source

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

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

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

Most severe consequence
 
3 prime UTR variant
Evidence status

Synonyms

Archive dbSNP rs58762896

This variant has 7 HGVS names - click the plus to show

About this variant

This variant overlaps 10 transcripts and has 2778 sample genotypes.

Variant displays