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: rs1057519823
rs1057519823 		15 66481830 missense variant T/C snv
CUI: C0027651
Disease: Neoplasms
Neoplasms 		Neoplasms 0.700 1.000 2 2009 2013
dbSNP: rs730880502
rs730880502 		15 66436762 missense variant T/A;G snv
CUI: C0027651
Disease: Neoplasms
Neoplasms 		Neoplasms 0.700 1.000 2 2009 2013
dbSNP: rs1057519820
rs1057519820 		15 66436810 missense variant A/C snv
CUI: C0027651
Disease: Neoplasms
Neoplasms 		Neoplasms 0.700 1.000 1 2009 2009
dbSNP: rs1057519821
rs1057519821 		15 66436814 missense variant G/C;T snv
CUI: C0027651
Disease: Neoplasms
Neoplasms 		Neoplasms 0.700 1.000 1 2009 2009
dbSNP: rs11629783
rs11629783 		15 66449049 intron variant C/A;G snv
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 1 2019 2019
dbSNP: rs1284398161
rs1284398161 		1.000 15 66485125 missense variant T/A snv
CUI: C4024896
Disease: Motor neuron atrophy
Motor neuron atrophy 		0.010 1.000 1 2012 2012
dbSNP: rs1489477346
rs1489477346 		15 66387359 synonymous variant G/A snv 5.8E-06 2.1E-05
CUI: C0027651
Disease: Neoplasms
Neoplasms 		Neoplasms 0.010 1.000 1 2012 2012
dbSNP: rs2053005
rs2053005 		15 66412111 intron variant G/A snv 6.5E-02
CUI: C0596887
Disease: mathematical ability
mathematical ability 		0.700 1.000 1 2018 2018
dbSNP: rs746354996
rs746354996 		15 66489734 missense variant G/A snv 2.8E-05 7.0E-06
CUI: C1608408
Disease: Malignant transformation
Malignant transformation 		0.010 1.000 1 2019 2019
dbSNP: rs730880508
rs730880508 		1.000 15 66436837 missense variant GC/TT mnv
CUI: C3809006
Disease: CARDIOFACIOCUTANEOUS SYNDROME 3
CARDIOFACIOCUTANEOUS SYNDROME 3 		0.700 0
dbSNP: rs1057519731
rs1057519731 		0.925 0.040 15 66436816 missense variant G/C snv
CUI: C0025202
Disease: melanoma
melanoma 		Neoplasms 0.720 1.000 5 2011 2014
dbSNP: rs1057519733
rs1057519733 		1.000 0.040 15 66481793 missense variant G/A snv
CUI: C0025202
Disease: melanoma
melanoma 		Neoplasms 0.700 1.000 3 2009 2013
dbSNP: rs1057519730
rs1057519730 		1.000 0.040 15 66436786 missense variant T/A;G snv
CUI: C0025202
Disease: melanoma
melanoma 		Neoplasms 0.700 1.000 2 2011 2012
dbSNP: rs1057519734
rs1057519734 		1.000 0.040 15 66485086 missense variant C/T snv
CUI: C0025202
Disease: melanoma
melanoma 		Neoplasms 0.700 1.000 2 2011 2012
dbSNP: rs1057519805
rs1057519805 		1.000 0.040 15 66436839 missense variant T/C snv
CUI: C0025202
Disease: melanoma
melanoma 		Neoplasms 0.700 1.000 2 2009 2013
dbSNP: rs1057519856
rs1057519856 		0.925 0.040 15 66436815 missense variant T/A snv
CUI: C0025202
Disease: melanoma
melanoma 		Neoplasms 0.020 1.000 2 2014 2014
dbSNP: rs1057519730
rs1057519730 		1.000 0.040 15 66436786 missense variant T/A;G snv
CUI: C0027651
Disease: Neoplasms
Neoplasms 		Neoplasms 0.700 1.000 1 2009 2009
dbSNP: rs1057519731
rs1057519731 		0.925 0.040 15 66436816 missense variant G/C snv
CUI: C0152013
Disease: Adenocarcinoma of lung (disorder)
Adenocarcinoma of lung (disorder) 		Neoplasms 0.700 1.000 1 2014 2014
dbSNP: rs1057519735
rs1057519735 		1.000 0.040 15 66490577 missense variant A/C snv
CUI: C0025202
Disease: melanoma
melanoma 		Neoplasms 0.700 1.000 1 2011 2011
dbSNP: rs1057519805
rs1057519805 		1.000 0.040 15 66436839 missense variant T/C snv
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm 		Neoplasms 0.010 1.000 1 2011 2011
dbSNP: rs1057519805
rs1057519805 		1.000 0.040 15 66436839 missense variant T/C snv
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms 		Neoplasms 0.010 1.000 1 2011 2011
dbSNP: rs1057519856
rs1057519856 		0.925 0.040 15 66436815 missense variant T/A snv
CUI: C0152013
Disease: Adenocarcinoma of lung (disorder)
Adenocarcinoma of lung (disorder) 		Neoplasms 0.700 1.000 1 2014 2014
dbSNP: rs1432441
rs1432441 		0.882 0.040 15 66426943 intron variant G/A snv 0.27
CUI: C1269683
Disease: Major Depressive Disorder
Major Depressive Disorder 		Mental Disorders 0.010 1.000 1 2017 2017
dbSNP: rs1432441
rs1432441 		0.882 0.040 15 66426943 intron variant G/A snv 0.27
CUI: C0041696
Disease: Unipolar Depression
Unipolar Depression 		Mental Disorders 0.010 1.000 1 2017 2017
dbSNP: rs1432441
rs1432441 		0.882 0.040 15 66426943 intron variant G/A snv 0.27
CUI: C0011581
Disease: Depressive disorder
Depressive disorder 		Mental Disorders 0.010 1.000 1 2017 2017