Original source

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

Alleles
A/G|Ancestral: A|Ambiguity code: R|MAF: 0.16 (G)
Location

Chromosome 11:102799093 (forward strand)|View in location tab

Co-located variant

HGMD-PUBLIC CR082027

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs386556557

HGVS names

This variant has 4 HGVS names - Hide

11:g.102799093A>G
ENST00000525739.6:n.682+971A>G
ENST00000371455.7:n.423+971A>G
ENST00000544704.1:n.443+971A>G

Genotyping chips

This variant has assays on 4 chips - Show

About this variant

This variant overlaps 4 transcripts, 1 regulatory feature, has 4024 sample genotypes and is mentioned in 3 citations.

Variant displays