Original source

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

Alleles
C/A | Ancestral: A | Ambiguity code: M | MAF: 0.26 (A)
Location

Chromosome 15:77673826 (forward strand) | View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs61014726, rs57444898

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

15:g.77673826C>A
ENST00000570216.5:c.-13+3263G>T
ENST00000559893.5:c.-13+3263G>T
ENST00000562933.5:c.-13+3263G>T
ENST00000563316.5:c.-13+3263G>T
ENST00000567726.5:c.-13+3263G>T
ENST00000561030.5:c.-13+3263G>T
ENST00000561686.5:c.-13+16894G>T
ENST00000566711.5:c.-13+3263G>T
ENST00000564472.5:c.-13+3263G>T

Genotyping chips

This variant has assays on: Affy GenomeWideSNP_6.0, Affy GeneChip 500K

About this variant

This variant overlaps 12 transcripts, has 4240 sample genotypes and is mentioned in 3 citations.

Variant displays