Original source

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

Alleles
G/A | Ancestral: G | Ambiguity code: R | MAF: 0.14 (A)
Location

Chromosome 13:113760228 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CS000454

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs36208072, rs563081

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