Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

Alleles
A/C | Ancestral: C | Ambiguity code: M | MAF: 0.28 (A)
Location

Chromosome 20:44436388 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs56973316, rs8121435

HGVS name

20:g.44436388A>C

This variation has assays on 10 chips - click the plus to show

About this variant

This variant overlaps 3 transcripts, has 3689 individual genotypes, is associated with 3 phenotypes and is mentioned in 9 citations.

Variation displays