Original source

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

Alleles
T/C | Ancestral: T | Ambiguity code: Y | MAF: 0.04 (C)
Location

Chromosome 11:34459518 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs17880098, rs36224103

HGVS name

11:g.34459518T>C

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

Variation displays