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: 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
dbSNP: rs2271397
rs2271397 		1.000 0.040 15 77615433 synonymous variant T/A;C snv 0.67
CUI: C0270736
Disease: Essential Tremor
Essential Tremor 		Nervous System Diseases 0.010 1.000 1 2013 2013
dbSNP: rs8028808
rs8028808 		1.000 0.040 15 77675074 intron variant G/A snv 0.23
CUI: C0270736
Disease: Essential Tremor
Essential Tremor 		Nervous System Diseases 0.010 1.000 1 2010 2010
dbSNP: rs9652490
rs9652490 		0.851 0.080 15 77671545 intron variant A/G snv 0.28
CUI: C4511452
Disease: Sporadic Parkinson disease
Sporadic Parkinson disease 		Nervous System Diseases 0.010 1.000 1 2010 2010
dbSNP: rs9652490
rs9652490 		0.851 0.080 15 77671545 intron variant A/G snv 0.28
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis 		Immune System Diseases; Nervous System Diseases 0.010 < 0.001 1 2013 2013