Original source

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

Alleles
G/A | Ancestral: G | Ambiguity code: R | MAF: 0.40 (A)
Location

Chromosome 20:63343128 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs60439625, rs17746134

HGVS name

20:g.63343128G>A

This variation has assays on 4 chips - click the plus to show

About this variant

This variant overlaps 8 transcripts, has 3027 individual genotypes and is mentioned in 4 citations.

Variation displays