Source: GWASCAT

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: rs2285803
rs2285803
PSORS1C1 ; PSORS1C2
0.925 0.160 6 31139481 intron variant T/C snv 0.72
CUI: C0026764
Disease: Multiple Myeloma
Multiple Myeloma 		0.810 1.000 1 2013 2014
dbSNP: rs3130573
rs3130573
PSORS1C1 ; PSORS1C2
1.000 0.040 6 31138491 non coding transcript exon variant A/C;G snv 8.1E-06; 0.33
CUI: C0036421
Disease: Systemic Scleroderma
Systemic Scleroderma 		0.800 1.000 1 2011 2011
dbSNP: rs3815087
rs3815087
PSORS1C1
0.851 0.200 6 31125810 5 prime UTR variant G/A snv 0.25
CUI: C1836230
Disease: HUMAN IMMUNODEFICIENCY VIRUS TYPE 1, SUSCEPTIBILITY TO
HUMAN IMMUNODEFICIENCY VIRUS TYPE 1, SUSCEPTIBILITY TO 		0.800 1.000 1 2009 2010
dbSNP: rs3815087
rs3815087
PSORS1C1
0.851 0.200 6 31125810 5 prime UTR variant G/A snv 0.25
CUI: C0038325
Disease: Stevens-Johnson Syndrome
Stevens-Johnson Syndrome 		0.800 1.000 1 2011 2011
dbSNP: rs3815087
rs3815087
PSORS1C1
0.851 0.200 6 31125810 5 prime UTR variant G/A snv 0.25
CUI: C1836232
Disease: ACQUIRED IMMUNODEFICIENCY SYNDROME, PROGRESSION TO
ACQUIRED IMMUNODEFICIENCY SYNDROME, PROGRESSION TO 		0.800 1.000 1 2009 2010
dbSNP: rs3815087
rs3815087
PSORS1C1
0.851 0.200 6 31125810 5 prime UTR variant G/A snv 0.25
CUI: C1836231
Disease: HIV-1, RESISTANCE TO
HIV-1, RESISTANCE TO 		0.800 1.000 1 2009 2010
dbSNP: rs3815087
rs3815087
PSORS1C1
0.851 0.200 6 31125810 5 prime UTR variant G/A snv 0.25
CUI: C1836233
Disease: AIDS, PROGRESSION TO
AIDS, PROGRESSION TO 		0.800 1.000 1 2009 2010
dbSNP: rs4959053
rs4959053
PSORS1C1
0.925 0.280 6 31131800 intron variant G/A snv 6.3E-02
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome 		0.800 1.000 1 2012 2013
dbSNP: rs1265097
rs1265097
PSORS1C1 ; PSORS1C2
6 31138682 missense variant C/A;T snv 0.13; 4.0E-06
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 3 2014 2019
dbSNP: rs149979052
rs149979052
PSORS1C1 ; PSORS1C2
1.000 0.040 6 31137370 intron variant C/T snv
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		0.700 1.000 2 2017 2019
dbSNP: rs1265091
rs1265091
PSORS1C1 ; PSORS1C2
6 31140352 upstream gene variant C/T snv 0.18
CUI: C0202230
Disease: Thyroid stimulating hormone measurement
Thyroid stimulating hormone measurement 		0.700 1.000 1 2018 2018
dbSNP: rs1265093
rs1265093
PSORS1C1 ; PSORS1C2
1.000 0.040 6 31139410 non coding transcript exon variant G/A snv 0.25
CUI: C0024117
Disease: Chronic Obstructive Airway Disease
Chronic Obstructive Airway Disease 		0.700 1.000 1 2012 2012
dbSNP: rs1265093
rs1265093
PSORS1C1 ; PSORS1C2
1.000 0.040 6 31139410 non coding transcript exon variant G/A snv 0.25
CUI: C3536958
Disease: Surfactant protein D measurement
Surfactant protein D measurement 		0.700 1.000 1 2012 2012
dbSNP: rs1265099
rs1265099
PSORS1C1 ; PSORS1C2
0.925 0.040 6 31137636 3 prime UTR variant A/G snv 0.41
CUI: C1269683
Disease: Major Depressive Disorder
Major Depressive Disorder 		0.700 1.000 1 2019 2019
dbSNP: rs1265099
rs1265099
PSORS1C1 ; PSORS1C2
0.925 0.040 6 31137636 3 prime UTR variant A/G snv 0.41
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		0.700 1.000 1 2019 2019
dbSNP: rs139332374
rs139332374
PSORS1C1
6 31134528 intron variant A/G snv
CUI: C0032181
Disease: Platelet Count measurement
Platelet Count measurement 		0.700 1.000 1 2018 2018
dbSNP: rs143933372
rs143933372
PSORS1C1
6 31131462 intron variant T/C snv 2.5E-03
CUI: C0201976
Disease: Creatinine measurement, serum (procedure)
Creatinine measurement, serum (procedure) 		0.700 1.000 1 2018 2018
dbSNP: rs149979052
rs149979052
PSORS1C1 ; PSORS1C2
1.000 0.040 6 31137370 intron variant C/T snv
CUI: C0008074
Disease: Child Development Disorders, Pervasive
Child Development Disorders, Pervasive 		0.700 1.000 1 2017 2017
dbSNP: rs16898823
rs16898823
PSORS1C1 ; PSORS1C2
6 31138829 non coding transcript exon variant A/T snv 0.14 0.11
CUI: C0202239
Disease: Uric acid measurement (procedure)
Uric acid measurement (procedure) 		0.700 1.000 1 2019 2019
dbSNP: rs2074478
rs2074478
PSORS1C1 ; PSORS1C2
1.000 0.040 6 31137856 3 prime UTR variant C/G;T snv
CUI: C0149745
Disease: Oral Ulcer
Oral Ulcer 		0.700 1.000 1 2019 2019
dbSNP: rs2233956
rs2233956
C6orf15 ; PSORS1C1
0.827 0.320 6 31113428 upstream gene variant T/C snv 0.12
CUI: C0017665
Disease: Membranous glomerulonephritis
Membranous glomerulonephritis 		0.700 1.000 1 2011 2011
dbSNP: rs2233956
rs2233956
C6orf15 ; PSORS1C1
0.827 0.320 6 31113428 upstream gene variant T/C snv 0.12
CUI: C0684249
Disease: Carcinoma of lung
Carcinoma of lung 		0.700 1.000 1 2017 2017
dbSNP: rs3094212
rs3094212
CDSN ; PSORS1C1
1.000 6 31117993 non coding transcript exon variant G/A snv 0.58
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure 		0.700 1.000 1 2010 2010
dbSNP: rs3094222
rs3094222
C6orf15 ; PSORS1C1
1.000 0.080 6 31113657 upstream gene variant A/G snv 9.7E-02
CUI: C0684249
Disease: Carcinoma of lung
Carcinoma of lung 		0.700 1.000 1 2017 2017
dbSNP: rs3095318
rs3095318
CDSN ; PSORS1C1
1.000 0.080 6 31120368 missense variant T/A;G snv 0.15; 4.7E-06
CUI: C0004096
Disease: Asthma
Asthma 		0.700 1.000 1 2017 2017