Original source

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

Alleles
C/T | Ancestral: T | Ambiguity code: Y | MAF: 0.28 (T)
Location

Chromosome 9:104902020 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs13301155

This variation has 4 HGVS names - click the plus to show

9:g.104902020C>T
ENST00000374733.1:c.-114-12825G>A
ENST00000374736.4:c.66+1594G>A
ENST00000423487.3:c.66+1594G>A

This variation has assays on 7 chips - click the plus to show

Variation displays