Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [View in dbSNP]

Alleles
T/C | Ancestral: C | Ambiguity code: Y | MAF: 0.13 (C)
Location

Chromosome 20:45925376 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs59009182

HGVS name

20:g.45925376T>C

This variation has assays on 10 chips - click the plus to show

About this variant

This variant overlaps 1 transcript, has 2242 individual genotypes, is associated with 6 phenotypes and is mentioned in 4 citations.

Variation displays