Original source

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

Alleles
T/C | Ancestral: T | Ambiguity code: Y | MAF: 0.16 (C)
Location

Chromosome 13:26957130 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs60996343

HGVS name

13:g.26957130T>C

This variation has assays on 11 chips - click the plus to show

Variation displays