Original source

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

Alleles
C/T|Ancestral: C|Ambiguity code: Y|MAF: 0.39 (T)
Location

Chromosome 3:15478737 (forward strand)|View in location tab

Most severe consequence
 
Non coding transcript exon variant
Evidence status

Synonyms

Archive dbSNP rs58526339, rs3773446

HGVS names

This variant has 7 HGVS names - Show

About this variant

This variant overlaps 7 transcripts and has 2779 sample genotypes.

Variant displays