Original source

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

C/A | Ancestral: A | Ambiguity code: M | MAF: 0.45 (C)

Chromosome 17:2799513 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs12952599

HGVS names

This variant has 5 HGVS names - Show

Genotyping chips

This variant has assays on: Illumina_HumanOmni2.5, Illumina_HumanOmni5

About this variant

This variant overlaps 4 transcripts and has 2514 sample genotypes.

Variant displays