Original source

Variants (including SNPs and indels) imported from dbSNP (release 138) | View in dbSNP

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

Chromosome 5:131992409 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CR097566

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs3756758, rs58550622

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

This variation has assays on 4 chips - click the plus to show

Variation displays