Original source

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

A/C | Ancestral: A | Ambiguity code: M | MAF: 0.20 (C)

Chromosome 5:132656717 (forward strand) | View in location tab


with HGMD-PUBLIC CR097566

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs3756758, rs58550622

HGVS names

This variant has 5 HGVS names - Show

Genotyping chips

This variant has assays on 5 chips - Show

About this variant

This variant overlaps 9 transcripts, 1 regulatory feature, has 3732 sample genotypes and is mentioned in 27 citations.

Variant displays