Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs12602950
rs12602950
CNP
17 41971811 non coding transcript exon variant G/A;C;T snv
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement 		0.700 1.000 1 2018 2018
dbSNP: rs2070106
rs2070106
CNP
0.925 0.160 17 41973846 synonymous variant G/A snv 0.31 0.25
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		0.050 1.000 5 2007 2018
dbSNP: rs1345128632
rs1345128632
CNP
0.925 0.080 17 41968217 synonymous variant G/A snv 7.0E-06
CUI: C0002736
Disease: Amyotrophic Lateral Sclerosis
Amyotrophic Lateral Sclerosis 		0.010 1.000 1 2007 2007
dbSNP: rs1345128632
rs1345128632
CNP
0.925 0.080 17 41968217 synonymous variant G/A snv 7.0E-06
CUI: C1611743
Disease: Familial (FPAH)
Familial (FPAH) 		0.010 1.000 1 2007 2007
dbSNP: rs2070106
rs2070106
CNP
0.925 0.160 17 41973846 synonymous variant G/A snv 0.31 0.25
CUI: C0004936
Disease: Mental disorders
Mental disorders 		0.010 1.000 1 2012 2012
dbSNP: rs2070106
rs2070106
CNP
0.925 0.160 17 41973846 synonymous variant G/A snv 0.31 0.25
CUI: C0007398
Disease: Catatonia
Catatonia 		0.010 1.000 1 2018 2018
dbSNP: rs2070106
rs2070106
CNP
0.925 0.160 17 41973846 synonymous variant G/A snv 0.31 0.25
CUI: C0033975
Disease: Psychotic Disorders
Psychotic Disorders 		0.010 1.000 1 2012 2012