Original source

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

Alleles
T/C | Ancestral: T | Ambiguity code: Y | MAF: 0.43 (T)
Location

Chromosome 9:89618028 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs60246708

HGVS name

9:g.89618028T>C

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

Variation displays