Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | 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
Evidence status

Synonyms

Archive dbSNP rs3172571, rs58158009

HGVS name

4:g.56393299C>A

This variation has assays on 8 chips - click the plus to show

About this variant

This variant overlaps 3 transcripts and has 4308 individual genotypes.

Variation displays