Original source

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

A/G | Ancestral: G | Ambiguity code: R | MAF: 0.46 (A)

Chromosome 19:10174102 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs17212459, rs57497454

HGVS names

This variant has 9 HGVS names - Show

Genotyping chips

This variant has assays on: Illumina_Human1M-duo, Illumina_HumanOmni5

About this variant

This variant overlaps 11 transcripts, has 3764 sample genotypes and is mentioned in 4 citations.

Variant displays