Original source

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

Alleles
G/A|Ancestral: A|Ambiguity code: R|MAF: 0.24 (A)
Location

Chromosome 15:77675074 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs61345969

HGVS names

This variant has 10 HGVS names - Hide

15:g.77675074G>A
ENST00000570216.5:c.-13+2015C>T
ENST00000559893.5:c.-13+2015C>T
ENST00000562933.5:c.-13+2015C>T
ENST00000563316.5:c.-13+2015C>T
ENST00000567726.5:c.-13+2015C>T
ENST00000561030.5:c.-13+2015C>T
ENST00000566711.5:c.-13+2015C>T
ENST00000561686.5:c.-13+15646C>T
ENST00000564472.5:c.-13+2015C>T

Genotyping chips

This variant has assays on 8 chips - Show

About this variant

This variant overlaps 12 transcripts, has 3763 sample genotypes and is mentioned in 3 citations.

Variant displays