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 (T)
Location

Chromosome 9:302324 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs57093748, rs785861, rs2484956

HGVS names

This variant has 13 HGVS names - Show

Genotyping chips

This variant has assays on: Affy GenomeWideSNP_6.0, Illumina_HumanOmni1-Quad

About this variant

This variant overlaps 11 transcripts and has 3966 sample genotypes.

Variant displays