Original source

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

Alleles
G/C | Ancestral: G | Ambiguity code: S | MAF: 0.40 (C)
Location

Chromosome 5:159395637 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs58850559

HGVS name

5:g.159395637G>C

This variation has assays on 5 chips - click the plus to show

About this variant

This variant has 2811 individual genotypes, is associated with 1 phenotype and is mentioned in 62 citations.

Variation displays