Original source

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

A/G | Ancestral: G | Ambiguity code: R | MAF: < 0.01 (A)

Chromosome 12:43761865 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs17619476, rs60179526

HGVS names

This variant has 15 HGVS names - Show

Genotyping chips

This variant has assays on: Illumina_Human1M-duo, Illumina_HumanOmni5

About this variant

This variant overlaps 21 transcripts and has 2628 sample genotypes.

Variant displays