STK38L, serine/threonine kinase 38 like, 23012

N. diseases: 12; N. variants: 3
Source: ALL
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs10842893
rs10842893
1.000 0.040 12 27269953 intron variant C/T snv 7.1E-02
CUI: C0017638
Disease: Glioma
Glioma
Neoplasms 0.710 1.000 1 2019 2019
dbSNP: rs12828220
rs12828220
12 27244859 intron variant T/C snv 0.44
CUI: C0596887
Disease: mathematical ability
mathematical ability
0.700 1.000 1 2018 2018
dbSNP: rs7358633
rs7358633
0.925 0.040 12 27261151 intron variant A/G snv 4.5E-02
SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3
0.700 1.000 1 2018 2018
dbSNP: rs7358633
rs7358633
0.925 0.040 12 27261151 intron variant A/G snv 4.5E-02
CUI: C0410702
Disease: Adolescent idiopathic scoliosis
Adolescent idiopathic scoliosis
Musculoskeletal Diseases 0.700 1.000 1 2018 2018