Original source

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

Alleles
T/C|Ambiguity code: Y|MAF: 0.07 (T)
Location

Chromosome 3:129059424 (forward strand)|View in location tab

Most severe consequence
 
Upstream gene variant
Evidence status

Synonyms

Archive dbSNP rs59925963

HGVS names

This variant has 2 HGVS names - Show

Genotyping chips

This variant has assays on 4 chips - Show

About this variant

This variant overlaps 2 transcripts and has 2838 sample genotypes.

Variant displays