Original source

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

G/A | Ancestral: G | Ambiguity code: R | MAF: 0.19 (A)

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


with HGMD-PUBLIC CS000454

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs36208072, rs563081

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

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

About this variant

This variant overlaps 6 transcripts, 1 regulatory feature, has 2592 sample genotypes and is mentioned in 2 citations.

Variant displays