Original source

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

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

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

Most severe consequence
 
Downstream gene variant
Evidence status

Synonyms

Archive dbSNP rs56973316, rs8121435

HGVS name

20:g.44436388A>C

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