Original source

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

Alleles
G/A | Ancestral: A | Ambiguity code: R | MAF: 0.33 (G)
Location

Chromosome 13:33623164 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CS043365

Most severe consequence
Evidence status

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

13:g.33623164G>A
ENST00000426690.2:c.-102-4740G>A
ENST00000380099.3:c.820-4740G>A
ENST00000487852.1:n.828-4740G>A

Genotyping chips

This variation has assays on: Illumina_HumanOmni1-Quad, Illumina_HumanOmni2.5, Illumina_HumanOmni5

Variation displays