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: 0.21 (C)
Location

Chromosome 9:22134095 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs60839437, rs56432185

HGVS name

9:g.22134095T>C

This variation has assays on 6 chips - click the plus to show

Variation displays