Original source

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

This variant has 10 HGVS names - click the plus to show

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
ENST00000566711.5:c.-13+5544T>C
ENST00000561686.5:c.-13+19175T>C
ENST00000564472.5:c.-13+5544T>C

This variant has assays on 12 chips - click the plus to show

About this variant

This variant overlaps 10 transcripts, has 3691 sample genotypes, is associated with 1 phenotype and is mentioned in 34 citations.

Variant displays