Original source

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

A/C | Ancestral: A | Ambiguity code: M | MAF: 0.34 (C)

Chromosome 3:46369003 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs72622924

HGVS names

This variant has 2 HGVS names - Show

Genotyping chips

This variant has assays on: Illumina_ImmunoChip

About this variant

This variant overlaps 3 transcripts, 1 regulatory feature, has 2508 sample genotypes and is mentioned in 3 citations.

Variant displays