Original source

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

Alleles
T/G | Ancestral: T | Ambiguity code: K | MAF: 0.37 (G)
Location

Chromosome 12:68808800 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CR043384

Most severe consequence
Evidence status

Clinical significance

This variation has 9 HGVS names - click the plus to show

12:g.68808800T>G
ENST00000393412.4:c.-5+309T>G
ENST00000258149.6:c.14+309T>G
ENST00000258148.8:c.14+309T>G
ENST00000462284.2:c.-5+309T>G
ENST00000311420.10:c.14+309T>G
ENST00000493419.1:n.210+309T>G
ENST00000393417.4:c.-5+309T>G
ENST00000428863.3:c.-5+309T>G

Genotyping chips

This variation has assays on: Illumina_HumanOmni1-Quad

Variation displays