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: rs25409
rs25409 		0.882 0.080 15 26773694 missense variant G/A snv 2.9E-03 3.5E-03
CUI: C0004352
Disease: Autistic Disorder
Autistic Disorder 		Mental Disorders 0.010 1.000 1 2011 2011
dbSNP: rs4906902
rs4906902 		0.724 0.200 15 26774621 intron variant A/G snv 0.15
CUI: C0014556
Disease: Epilepsy, Temporal Lobe
Epilepsy, Temporal Lobe 		Nervous System Diseases 0.010 1.000 1 2011 2011
dbSNP: rs4906902
rs4906902 		0.724 0.200 15 26774621 intron variant A/G snv 0.15
CUI: C0014548
Disease: Epilepsy, Generalized
Epilepsy, Generalized 		Nervous System Diseases 0.010 1.000 1 2011 2011
dbSNP: rs4906902
rs4906902 		0.724 0.200 15 26774621 intron variant A/G snv 0.15
CUI: C0344315
Disease: Depressed mood
Depressed mood 		Behavior and Behavior Mechanisms 0.010 1.000 1 2011 2011
dbSNP: rs4906902
rs4906902 		0.724 0.200 15 26774621 intron variant A/G snv 0.15
CUI: C0011581
Disease: Depressive disorder
Depressive disorder 		Mental Disorders 0.010 1.000 1 2011 2011
dbSNP: rs4906902
rs4906902 		0.724 0.200 15 26774621 intron variant A/G snv 0.15
CUI: C0011570
Disease: Mental Depression
Mental Depression 		Behavior and Behavior Mechanisms 0.010 1.000 1 2011 2011
dbSNP: rs878960
rs878960 		0.925 0.040 15 26683789 intron variant C/G;T snv
CUI: C3840214
Disease: High-functioning autism
High-functioning autism 		Mental Disorders 0.010 1.000 1 2011 2011
dbSNP: rs878960
rs878960 		0.925 0.040 15 26683789 intron variant C/G;T snv
CUI: C0236792
Disease: Asperger Syndrome
Asperger Syndrome 		Mental Disorders 0.010 1.000 1 2011 2011
dbSNP: rs886037938
rs886037938 		1.000 15 26621417 missense variant C/T snv
CUI: C4310712
Disease: EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 43
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 43 		0.800 1.000 6 2013 2017
dbSNP: rs886037939
rs886037939 		1.000 15 26580456 missense variant T/A snv
CUI: C4310712
Disease: EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 43
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 43 		0.800 1.000 6 2013 2017
dbSNP: rs886037940
rs886037940 		1.000 15 26567671 missense variant G/T snv
CUI: C4310712
Disease: EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 43
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 43 		0.800 1.000 6 2013 2017
dbSNP: rs886037941
rs886037941 		1.000 15 26561099 missense variant C/T snv
CUI: C4310712
Disease: EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 43
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 43 		0.800 1.000 6 2013 2017
dbSNP: rs11631129
rs11631129 		15 26732026 intron variant G/A;C snv
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2013 2013
dbSNP: rs12910337
rs12910337 		15 26748096 intron variant C/T snv 0.91
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2013 2013
dbSNP: rs3212332
rs3212332 		15 26768806 intron variant T/A snv 0.91
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2013 2013
dbSNP: rs3212343
rs3212343 		15 26764379 intron variant T/A;C snv
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2013 2013
dbSNP: rs4392030
rs4392030 		15 26777184 intron variant G/C snv 0.89
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2013 2013
dbSNP: rs4632102
rs4632102 		15 26789887 non coding transcript exon variant C/T snv 0.90
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2013 2013
dbSNP: rs4906898
rs4906898 		15 26733600 intron variant A/C;T snv
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2013 2013
dbSNP: rs4906904
rs4906904 		15 26788938 intron variant A/C;G;T snv
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2013 2013
dbSNP: rs4906905
rs4906905 		15 26789098 intron variant T/A snv 0.89
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2013 2013
dbSNP: rs4906906
rs4906906 		15 26789376 intron variant A/C;T snv
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2013 2013
dbSNP: rs6576604
rs6576604 		15 26750050 non coding transcript exon variant A/G;T snv
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2013 2013
dbSNP: rs6576606
rs6576606 		15 26762437 intron variant A/G;T snv
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2013 2013
dbSNP: rs6576611
rs6576611 		15 26789146 intron variant T/A;C snv
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2013 2013