Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [View in dbSNP]

A/C | Ancestral: A | Ambiguity code: M | MAF: 0.36 (C)

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

Most severe consequence
Evidence status


Archive dbSNP rs72622924

This variation has 2 HGVS names - click the plus to show

Genotyping chips

This variation has assays on: Illumina_ImmunoChip

About this variant

This variant overlaps 4 transcripts, has 1098 individual genotypes and is mentioned in 3 citations.

Variation displays