Original source

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

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

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

Most severe consequence
 
Intron variant
Evidence status

Synonyms

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