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: rs750612085
rs750612085 		1.000 15 77615044 missense variant T/C snv 1.2E-05
CUI: C4748192
Disease: MENTAL RETARDATION, AUTOSOMAL RECESSIVE 64
MENTAL RETARDATION, AUTOSOMAL RECESSIVE 64 		0.800 1.000 1 2018 2018
dbSNP: rs757077698
rs757077698 		1.000 15 77615038 missense variant C/T snv 2.8E-05
CUI: C4748192
Disease: MENTAL RETARDATION, AUTOSOMAL RECESSIVE 64
MENTAL RETARDATION, AUTOSOMAL RECESSIVE 64 		0.800 1.000 1 2018 2018
dbSNP: rs11629474
rs11629474 		1.000 0.040 15 77771243 intron variant A/C snv 0.19
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs11629621
rs11629621 		1.000 0.040 15 77788395 non coding transcript exon variant C/G snv 0.56
CUI: C1269683
Disease: Major Depressive Disorder
Major Depressive Disorder 		Mental Disorders 0.700 1.000 1 2018 2018
dbSNP: rs11855853
rs11855853 		15 77720276 intron variant C/T snv 0.21
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 1 2019 2019
dbSNP: rs11856579
rs11856579 		15 77720346 intron variant G/A snv 0.23
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 1 2019 2019
dbSNP: rs12324894
rs12324894 		1.000 0.040 15 77740365 intron variant G/A snv 0.11
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs12592419
rs12592419 		1.000 0.040 15 77772882 intron variant G/A;T snv
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs12905542
rs12905542 		1.000 0.040 15 77745782 intron variant A/C;T snv
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs3935685
rs3935685 		15 77741926 intron variant T/C snv 0.37
CUI: C0021704
Disease: Intelligence
Intelligence 		Behavior and Behavior Mechanisms 0.700 1.000 1 2019 2019
dbSNP: rs3935685
rs3935685 		15 77741926 intron variant T/C snv 0.37
CUI: C0596887
Disease: mathematical ability
mathematical ability 		0.700 1.000 1 2018 2018
dbSNP: rs3936093
rs3936093 		1.000 0.040 15 77809567 intron variant A/G snv 0.47
CUI: C1269683
Disease: Major Depressive Disorder
Major Depressive Disorder 		Mental Disorders 0.700 1.000 1 2018 2018
dbSNP: rs3936093
rs3936093 		1.000 0.040 15 77809567 intron variant A/G snv 0.47
CUI: C0525045
Disease: Mood Disorders
Mood Disorders 		Mental Disorders 0.700 1.000 1 2018 2018
dbSNP: rs4468571
rs4468571 		1.000 0.040 15 77727790 intron variant A/G snv 0.35
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		Mental Disorders 0.700 1.000 1 2019 2019
dbSNP: rs4468571
rs4468571 		1.000 0.040 15 77727790 intron variant A/G snv 0.35
CUI: C0021704
Disease: Intelligence
Intelligence 		Behavior and Behavior Mechanisms 0.700 1.000 1 2019 2019
dbSNP: rs62007784
rs62007784 		15 77742361 intron variant C/T snv 0.37
CUI: C0596887
Disease: mathematical ability
mathematical ability 		0.700 1.000 1 2018 2018
dbSNP: rs62007820
rs62007820 		15 77768444 intron variant G/A snv 0.21
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement 		0.700 1.000 1 2019 2019
dbSNP: rs7162468
rs7162468 		1.000 0.040 15 77756650 intron variant C/A;T snv 0.20
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs7170398
rs7170398 		1.000 0.040 15 77775291 intron variant C/T snv 0.35
CUI: C1269683
Disease: Major Depressive Disorder
Major Depressive Disorder 		Mental Disorders 0.700 1.000 1 2018 2018
dbSNP: rs7175083
rs7175083 		1.000 0.040 15 77714500 intron variant T/C snv 0.50
CUI: C0525045
Disease: Mood Disorders
Mood Disorders 		Mental Disorders 0.700 1.000 1 2018 2018
dbSNP: rs7175083
rs7175083 		1.000 0.040 15 77714500 intron variant T/C snv 0.50
CUI: C1269683
Disease: Major Depressive Disorder
Major Depressive Disorder 		Mental Disorders 0.700 1.000 1 2018 2018
dbSNP: rs11856808
rs11856808 		0.827 0.120 15 77680428 intron variant C/T snv 0.42
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis 		Immune System Diseases; Nervous System Diseases 0.010 < 0.001 1 2013 2013
dbSNP: rs11856808
rs11856808 		0.827 0.120 15 77680428 intron variant C/T snv 0.42
CUI: C2609259
Disease: Symphysis Pubis Dysfunction
Symphysis Pubis Dysfunction 		Pathological Conditions, Signs and Symptoms 0.010 < 0.001 1 2010 2010
dbSNP: rs11856808
rs11856808 		0.827 0.120 15 77680428 intron variant C/T snv 0.42
CUI: C1611743
Disease: Familial (FPAH)
Familial (FPAH) 		0.010 1.000 1 2012 2012
dbSNP: rs13313467
rs13313467 		1.000 0.040 15 77673826 intron variant C/A snv 0.28
CUI: C0270736
Disease: Essential Tremor
Essential Tremor 		Nervous System Diseases 0.010 1.000 1 2010 2010