Original source

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

Alleles
C/A|Ancestral: C|Ambiguity code: M|MAF: 0.23 (A)
Location

Chromosome 4:56393299 (forward strand)|View in location tab

Most severe consequence
 
Upstream gene variant
Evidence status

Synonyms

Archive dbSNP rs3172571, rs58158009

HGVS name

4:g.56393299C>A

Genotyping chips

This variant has assays on 8 chips - Show

About this variant

This variant overlaps 3 transcripts and has 4308 sample genotypes.

Variant displays