Original source

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

Alleles
G/A/T|Ancestral: G|Ambiguity code: D|MAF: < 0.01 (T)
Location

Chromosome 9:127912633 (forward strand)|View in location tab

Co-located variant

COSMIC COSM3685503

Most severe consequence
 
Synonymous variant
Evidence status

HGVS names

This variant has 14 HGVS names - Show

Genotyping chips

This variant has assays on: Illumina_Human1M-duo, Illumina_HumanOmni5

About this variant

This variant overlaps 14 transcripts and has 3240 sample genotypes.

Variant displays