Original source

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

Alleles
T/G | Ancestral: G | Ambiguity code: K | MAF: 0.28 (T)
Location

Chromosome 20:5301690 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs58483966

HGVS name

20:g.5301690T>G

About this variant

This variant overlaps 1 transcript and has 2512 individual genotypes.

Variation displays