Original source

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

Alleles
A/C|Ancestral: C|Ambiguity code: M|MAF: 0.24 (C)
Location

Chromosome 3:16586299 (forward strand)|View in location tab

Most severe consequence
 
Downstream gene variant
Evidence status

Synonyms

Archive dbSNP rs58146551

HGVS name

3:g.16586299A>C

Genotyping chips

This variant has assays on 12 chips - Show

About this variant

This variant overlaps 2 transcripts and has 5736 sample genotypes.

Variant displays