RAB38, RAB38, member RAS oncogene family, 23682

N. diseases: 34; N. variants: 17
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: rs302668
rs302668
0.925 0.120 11 88143743 intron variant T/C snv 0.28
CUI: C0338451
Disease: Frontotemporal dementia
Frontotemporal dementia
Nutritional and Metabolic Diseases; Nervous System Diseases; Mental Disorders 0.810 1.000 1 2014 2014
dbSNP: rs10501658
rs10501658
1.000 0.040 11 88055724 intron variant A/C snv 6.2E-02
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute
Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs10831205
rs10831205
1.000 0.040 11 88068689 intron variant A/C;G snv
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute
Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs116951285
rs116951285
11 88124996 intron variant T/A;C snv 1.3E-02
CUI: C0428419
Disease: Triiodothyronine measurement
Triiodothyronine measurement
0.700 1.000 1 2019 2019
dbSNP: rs16914161
rs16914161
1.000 0.040 11 88057358 intron variant T/C;G snv
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute
Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs2220303
rs2220303
1.000 0.040 11 88058268 intron variant G/A;C;T snv
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute
Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs534692
rs534692
1.000 0.040 11 88051176 intron variant G/A;C snv
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute
Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs545489
rs545489
1.000 0.040 11 88060179 intron variant G/A snv 0.59
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute
Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs555354
rs555354
1.000 0.040 11 88056247 intron variant T/A snv 0.43
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute
Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs632483
rs632483
1.000 0.040 11 88057817 intron variant G/A snv 0.59
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute
Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs642007
rs642007
1.000 0.040 11 88063975 intron variant A/C snv 0.75
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute
Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs659026
rs659026
1.000 0.040 11 88065396 intron variant T/C snv 0.47
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute
Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs7935712
rs7935712
1.000 0.040 11 88051253 intron variant T/A snv 0.62
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute
Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs7945438
rs7945438
1.000 0.040 11 88050112 non coding transcript exon variant G/A snv 0.89
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute
Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs953353
rs953353
1.000 0.040 11 88061005 intron variant C/T snv 0.78
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute
Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs988975
rs988975
1.000 0.040 11 88058319 intron variant T/C snv 0.62
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute
Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs302668
rs302668
0.925 0.120 11 88143743 intron variant T/C snv 0.28
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease
Nervous System Diseases; Mental Disorders 0.010 1.000 1 2016 2016
dbSNP: rs9144
rs9144
1.000 0.040 11 88113589 3 prime UTR variant C/A;T snv
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
Digestive System Diseases 0.010 1.000 1 2019 2019