Original source

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

A/C/G | Ancestral: A | Ambiguity code: V | MAF: 0.38 (A)

Chromosome 12:90964479 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs60128188

HGVS names

This variant has 4 HGVS names - Show

Genotyping chips

This variant has assays on: Illumina_Human1M-duo, Illumina_HumanOmni2.5, Illumina_HumanOmni5

About this variant

This variant overlaps 2 transcripts and has 2782 sample genotypes.

Variant displays