Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|View in dbSNP

Alleles
T/C|Ancestral: C|Ambiguity code: Y|MAF: 0.12 (C)
Location

Chromosome 9:121332522 (forward strand)|View in location tab

Most severe consequence
 
Synonymous variant
Evidence status

Synonyms

Archive dbSNP rs3191330, rs1050966

HGVS names

This variant has 21 HGVS names - Show

Genotyping chips

This variant has assays on: Illumina_ImmunoChip, Illumina_HumanOmni1-Quad, Illumina_HumanOmni5

About this variant

Variant displays