Original source

Variants (including SNPs and indels) imported from dbSNP (release 138) | View in dbSNP

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

Chromosome 5:158822645 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs58850559

HGVS name

5:g.158822645G>C

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

Variation displays