Original source

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

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

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

Co-located

with HGMD-PUBLIC CS000454

Most severe consequence
 
Intron variant
Evidence status

Synonyms

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