Original source

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

Alleles
T/C|Ancestral: C|Ambiguity code: Y|MAF: 0.13 (C)
Location

Chromosome 16:1509964 (forward strand)|View in location tab

Most severe consequence
 
3 prime UTR variant
Evidence status

Synonyms

Archive dbSNP rs56689278

HGVS names

This variant has 3 HGVS names - Show

About this variant

This variant overlaps 13 transcripts and has 2507 sample genotypes.

Variant displays