Original source

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

Synonyms

Archive dbSNP rs61345969

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

15:g.77675074G>A
ENST00000570216.2:c.-13+2015C>T
ENST00000559893.2:c.-13+2015C>T
ENST00000562933.2:c.-13+2015C>T
ENST00000563316.2:c.-13+2015C>T
ENST00000567726.2:c.-13+2015C>T
ENST00000561030.2:c.-13+2015C>T
ENST00000561686.2:c.-13+15646C>T
ENST00000566711.2:c.-13+2015C>T
ENST00000564472.2:c.-13+2015C>T

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

Variation displays