Original source

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

Alleles
A/G|Ancestral: G|Ambiguity code: R|MAF: 0.48 (G)
Location

Chromosome 3:184378790 (forward strand)|View in location tab

Co-located variant

HGMD-PUBLIC CR084015

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs57526857, rs386619456

HGVS names

This variant has 2 HGVS names - Show

Genotyping chips

This variant has assays on 8 chips - Show

About this variant

This variant overlaps 20 transcripts, 1 regulatory feature, has 3795 sample genotypes and is mentioned in 1 citation.

Variant displays