Original source

Variants (including SNPs and indels) imported from dbSNP (release 138) | View in dbSNP

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

Chromosome 15:77966168 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs61014726, rs57444898

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

15:g.77966168C>A
ENST00000570216.1:c.-13+3263G>T
ENST00000559893.1:c.-13+3263G>T
ENST00000562933.1:c.-13+3263G>T
ENST00000563316.1:c.-13+3263G>T
ENST00000567726.1:c.-13+3263G>T
ENST00000561030.1:c.-13+3263G>T
ENST00000561686.1:c.-13+16894G>T
ENST00000566711.1:c.-13+3263G>T
ENST00000564472.1:c.-13+3263G>T

Genotyping chips

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

Variation displays