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: 0.20 (C)

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


with HGMD-PUBLIC CR097566

Most severe consequence
Evidence status


Archive dbSNP rs3756758, rs58550622

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

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

About this variant

This variant overlaps 10 transcripts, has 2330 individual genotypes and is mentioned in 24 citations.

Variation displays