Original source

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

with HGMD-PUBLIC CR082027

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs386556557

This variant has 4 HGVS names - click the plus to show

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

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

About this variant

This variant overlaps 4 transcripts, 1 regulatory feature, has 2568 sample genotypes and is mentioned in 3 citations.

Variant displays