Original source

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

Alleles
A/G|Ancestral: G|Ambiguity code: R|MAF: 0.27 (G)
Location

Chromosome 15:77671545 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs59418404

HGVS names

This variant has 10 HGVS names - Hide

15:g.77671545A>G
ENST00000570216.5:c.-13+5544T>C
ENST00000559893.5:c.-13+5544T>C
ENST00000562933.5:c.-13+5544T>C
ENST00000563316.5:c.-13+5544T>C
ENST00000567726.5:c.-13+5544T>C
ENST00000561030.5:c.-13+5544T>C
ENST00000561686.5:c.-13+19175T>C
ENST00000566711.5:c.-13+5544T>C
ENST00000564472.5:c.-13+5544T>C

Genotyping chips

This variant has assays on 12 chips - Show

About this variant

This variant overlaps 10 transcripts, has 3691 sample genotypes, is associated with 1 phenotype and is mentioned in 33 citations.

Variant displays