Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [View in dbSNP]

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

Chromosome 13:113105914 (forward strand) | View in location tab


with HGMD-PUBLIC CS000454

Most severe consequence
Evidence status


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

About this variant

This variant overlaps 7 transcripts, has 1186 individual genotypes and is mentioned in 2 citations.

Variation displays