Original source

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

HGVS names

This variant has 10 HGVS names - Hide

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