Source: CURATED

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: rs2260000
rs2260000
PRRC2A
0.851 0.200 6 31625699 intron variant A/G snv 0.29
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis 		0.700 1.000 3 2007 2011
dbSNP: rs115052633
rs115052633
PRRC2A ; SNORA38
1.000 0.040 6 31621487 intron variant C/G;T snv
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		0.700 1.000 1 2017 2017
dbSNP: rs115052633
rs115052633
PRRC2A ; SNORA38
1.000 0.040 6 31621487 intron variant C/G;T snv
CUI: C0008074
Disease: Child Development Disorders, Pervasive
Child Development Disorders, Pervasive 		0.700 1.000 1 2017 2017
dbSNP: rs2242660
rs2242660
PRRC2A
0.925 0.160 6 31629976 intron variant G/A snv 0.46
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic 		0.700 1.000 1 2014 2014
dbSNP: rs2242660
rs2242660
PRRC2A
0.925 0.160 6 31629976 intron variant G/A snv 0.46
CUI: C0019829
Disease: Hodgkin Disease
Hodgkin Disease 		0.700 1.000 1 2013 2013
dbSNP: rs2260000
rs2260000
PRRC2A
0.851 0.200 6 31625699 intron variant A/G snv 0.29
CUI: C1836231
Disease: HIV-1, RESISTANCE TO
HIV-1, RESISTANCE TO 		0.700 1.000 1 2010 2010
dbSNP: rs2260000
rs2260000
PRRC2A
0.851 0.200 6 31625699 intron variant A/G snv 0.29
CUI: C1836232
Disease: ACQUIRED IMMUNODEFICIENCY SYNDROME, PROGRESSION TO
ACQUIRED IMMUNODEFICIENCY SYNDROME, PROGRESSION TO 		0.700 1.000 1 2010 2010
dbSNP: rs2260000
rs2260000
PRRC2A
0.851 0.200 6 31625699 intron variant A/G snv 0.29
CUI: C1836230
Disease: HUMAN IMMUNODEFICIENCY VIRUS TYPE 1, SUSCEPTIBILITY TO
HUMAN IMMUNODEFICIENCY VIRUS TYPE 1, SUSCEPTIBILITY TO 		0.700 1.000 1 2010 2010
dbSNP: rs2260000
rs2260000
PRRC2A
0.851 0.200 6 31625699 intron variant A/G snv 0.29
CUI: C1836233
Disease: AIDS, PROGRESSION TO
AIDS, PROGRESSION TO 		0.700 1.000 1 2010 2010
dbSNP: rs2260000
rs2260000
PRRC2A
0.851 0.200 6 31625699 intron variant A/G snv 0.29
CUI: C0011854
Disease: Diabetes Mellitus, Insulin-Dependent
Diabetes Mellitus, Insulin-Dependent 		0.700 1.000 1 2007 2007
dbSNP: rs2736157
rs2736157
PRRC2A ; MIR6832
1.000 0.120 6 31633043 intron variant A/G;T snv 0.15 0.17
CUI: C0149678
Disease: Epstein-Barr Virus Infections
Epstein-Barr Virus Infections 		0.700 1.000 1 2013 2013
dbSNP: rs2736157
rs2736157
PRRC2A ; MIR6832
1.000 0.120 6 31633043 intron variant A/G;T snv 0.15 0.17
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis 		0.700 1.000 1 2011 2011
dbSNP: rs2736171
rs2736171
PRRC2A
0.925 0.120 6 31627710 intron variant A/G snv 0.34
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis 		0.700 1.000 1 2011 2011
dbSNP: rs2736171
rs2736171
PRRC2A
0.925 0.120 6 31627710 intron variant A/G snv 0.34
CUI: C1836230
Disease: HUMAN IMMUNODEFICIENCY VIRUS TYPE 1, SUSCEPTIBILITY TO
HUMAN IMMUNODEFICIENCY VIRUS TYPE 1, SUSCEPTIBILITY TO 		0.700 1.000 1 2010 2010
dbSNP: rs2736171
rs2736171
PRRC2A
0.925 0.120 6 31627710 intron variant A/G snv 0.34
CUI: C1836233
Disease: AIDS, PROGRESSION TO
AIDS, PROGRESSION TO 		0.700 1.000 1 2010 2010
dbSNP: rs2736171
rs2736171
PRRC2A
0.925 0.120 6 31627710 intron variant A/G snv 0.34
CUI: C1836231
Disease: HIV-1, RESISTANCE TO
HIV-1, RESISTANCE TO 		0.700 1.000 1 2010 2010
dbSNP: rs2736171
rs2736171
PRRC2A
0.925 0.120 6 31627710 intron variant A/G snv 0.34
CUI: C1836232
Disease: ACQUIRED IMMUNODEFICIENCY SYNDROME, PROGRESSION TO
ACQUIRED IMMUNODEFICIENCY SYNDROME, PROGRESSION TO 		0.700 1.000 1 2010 2010
dbSNP: rs2736173
rs2736173
PRRC2A ; SNORA38
1.000 0.080 6 31621958 intron variant C/T snv 1.7E-02
CUI: C0039263
Disease: Takayasu Arteritis
Takayasu Arteritis 		0.700 1.000 1 2015 2015
dbSNP: rs2844472
rs2844472
PRRC2A ; SNORA38
0.925 0.120 6 31621899 intron variant A/G snv 0.29
CUI: C1836233
Disease: AIDS, PROGRESSION TO
AIDS, PROGRESSION TO 		0.700 1.000 1 2010 2010
dbSNP: rs2844472
rs2844472
PRRC2A ; SNORA38
0.925 0.120 6 31621899 intron variant A/G snv 0.29
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis 		0.700 1.000 1 2011 2011
dbSNP: rs2844472
rs2844472
PRRC2A ; SNORA38
0.925 0.120 6 31621899 intron variant A/G snv 0.29
CUI: C1836232
Disease: ACQUIRED IMMUNODEFICIENCY SYNDROME, PROGRESSION TO
ACQUIRED IMMUNODEFICIENCY SYNDROME, PROGRESSION TO 		0.700 1.000 1 2010 2010
dbSNP: rs2844472
rs2844472
PRRC2A ; SNORA38
0.925 0.120 6 31621899 intron variant A/G snv 0.29
CUI: C1836230
Disease: HUMAN IMMUNODEFICIENCY VIRUS TYPE 1, SUSCEPTIBILITY TO
HUMAN IMMUNODEFICIENCY VIRUS TYPE 1, SUSCEPTIBILITY TO 		0.700 1.000 1 2010 2010
dbSNP: rs2844472
rs2844472
PRRC2A ; SNORA38
0.925 0.120 6 31621899 intron variant A/G snv 0.29
CUI: C1836231
Disease: HIV-1, RESISTANCE TO
HIV-1, RESISTANCE TO 		0.700 1.000 1 2010 2010
dbSNP: rs3130070
rs3130070
PRRC2A
6 31624031 intron variant A/G snv 0.17
CUI: C0149678
Disease: Epstein-Barr Virus Infections
Epstein-Barr Virus Infections 		0.700 1.000 1 2013 2013
dbSNP: rs3130623
rs3130623
PRRC2A
6 31629923 intron variant C/T snv 0.18
CUI: C0149678
Disease: Epstein-Barr Virus Infections
Epstein-Barr Virus Infections 		0.700 1.000 1 2013 2013