Original source

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

Alleles
T/G | Ancestral: T | Ambiguity code: K | MAF: 0.19 (G)
Location

Chromosome 7:22862626 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs59152366

HGVS name

7:g.22862626T>G

This variation has assays on 8 chips - click the plus to show

Variation displays