RAVER2, ribonucleoprotein, PTB binding 2, 55225

N. diseases: 8; N. variants: 7
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: rs12752552
rs12752552
0.882 0.040 1 64763616 intron variant T/C snv 0.13
CUI: C0017638
Disease: Glioma
Glioma
Neoplasms 0.700 1.000 2 2017 2018
dbSNP: rs114695117
rs114695117
1 64743428 upstream gene variant C/A;T snv
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure
0.700 1.000 1 2016 2016
dbSNP: rs12752552
rs12752552
0.882 0.040 1 64763616 intron variant T/C snv 0.13
CUI: C0017636
Disease: Glioblastoma
Glioblastoma
Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs12752552
rs12752552
0.882 0.040 1 64763616 intron variant T/C snv 0.13
CUI: C0085136
Disease: Central Nervous System Neoplasms
Central Nervous System Neoplasms
Neoplasms; Nervous System Diseases 0.700 1.000 1 2017 2017
dbSNP: rs12752552
rs12752552
0.882 0.040 1 64763616 intron variant T/C snv 0.13
CUI: C1621958
Disease: Glioblastoma Multiforme
Glioblastoma Multiforme
Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs9128
rs9128
1 64833288 3 prime UTR variant C/T snv 7.6E-03
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 1 2019 2019
dbSNP: rs112395617
rs112395617
1.000 0.080 1 64833868 3 prime UTR variant -/TTAA;TTAATTAA delins
CUI: C2239176
Disease: Liver carcinoma
Liver carcinoma
Digestive System Diseases; Neoplasms 0.010 1.000 1 2018 2018
dbSNP: rs1333739
rs1333739
1 64827766 intron variant A/G;T snv 0.62
CUI: C0004364
Disease: Autoimmune Diseases
Autoimmune Diseases
Immune System Diseases 0.010 1.000 1 2012 2012
dbSNP: rs2780814
rs2780814
1.000 0.040 1 64827272 intron variant C/G;T snv
CUI: C0004364
Disease: Autoimmune Diseases
Autoimmune Diseases
Immune System Diseases 0.010 1.000 1 2012 2012
dbSNP: rs2780814
rs2780814
1.000 0.040 1 64827272 intron variant C/G;T snv
CUI: C0009324
Disease: Ulcerative Colitis
Ulcerative Colitis
Digestive System Diseases 0.010 1.000 1 2012 2012
dbSNP: rs2780889
rs2780889
1 64833108 3 prime UTR variant A/T snv 0.52
CUI: C0004364
Disease: Autoimmune Diseases
Autoimmune Diseases
Immune System Diseases 0.010 1.000 1 2012 2012