Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | 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

This variant has 5 HGVS names - click the plus to show

This variant has assays on 5 chips - click the plus to show

About this variant

This variant overlaps 9 transcripts, 1 regulatory feature, has 2613 sample genotypes and is mentioned in 26 citations.

Variant displays