Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|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 variant

HGMD-PUBLIC CS000454

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs36208072, rs563081

HGVS names

This variant has 8 HGVS names - Show

Genotyping chips

This variant has assays on 4 chips - Show

About this variant

This variant overlaps 8 transcripts, 1 regulatory feature, has 2592 sample genotypes and is mentioned in 2 citations.

Variant displays