Original source

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

Alleles
T/G | Ancestral: G | Ambiguity code: K | MAF: 0.22 (G)
Location

Chromosome 20:5316005 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs58194117, rs17721333

HGVS name

20:g.5316005T>G

This variation has assays on 7 chips - click the plus to show

About this variant

This variant overlaps 1 transcript and has 3763 individual genotypes.

Variation displays