Original source

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

A/G | Ancestral: A | Ambiguity code: R | MAF: 0.43 (G)

Chromosome 22:41993835 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs74278442, rs59948179

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 12 transcripts and has 2779 sample genotypes.

Variant displays