Original source

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

Alleles
T/C | Ancestral: C | Ambiguity code: Y | MAF: 0.32 (T)
Location

Chromosome 19:30289289 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs60808716, rs12982313

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

19:g.30289289T>C
ENST00000591488.1:c.-120+60616T>C
ENST00000585628.3:c.-120+5148T>C
ENST00000590564.3:n.454+5148T>C

This variation has assays on 9 chips - click the plus to show

Variation displays