Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [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
Evidence status

Synonyms

Archive dbSNP rs61014726, rs57444898

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

15:g.77673826C>A
ENST00000570216.3:c.-13+3263G>T
ENST00000559893.3:c.-13+3263G>T
ENST00000562933.3:c.-13+3263G>T
ENST00000563316.3:c.-13+3263G>T
ENST00000567726.3:c.-13+3263G>T
ENST00000561030.3:c.-13+3263G>T
ENST00000566711.3:c.-13+3263G>T
ENST00000561686.3:c.-13+16894G>T
ENST00000564472.3:c.-13+3263G>T

Genotyping chips

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

Variation displays