Original source

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

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

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

Most severe consequence
Downstream gene variant
Evidence status


Archive dbSNP rs56973316, rs8121435

HGVS name


Genotyping chips

This variant has assays on 10 chips - Show

About this variant

This variant overlaps 2 transcripts, 1 regulatory feature, has 3689 sample genotypes, is associated with 3 phenotypes and is mentioned in 8 citations.

Variant displays