Original source

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

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

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

This variant has assays on 8 chips - click the plus to show

About this variant

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

Variant displays