Original source

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

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

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

Most severe consequence
Intron variant
Evidence status


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