Source: GWASDB

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: rs111611512
rs111611512 		Y 11313671 upstream gene variant T/A;C;G snv
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2012 2012
dbSNP: rs36141869
rs36141869 		1.000 0.040 Y 19115754 intergenic variant T/C snv
CUI: C0700639
Disease: Pyloric Stenosis, Hypertrophic
Pyloric Stenosis, Hypertrophic 		0.700 1.000 1 2012 2012
dbSNP: rs5945326
rs5945326 		0.925 0.080 X 153634467 regulatory region variant A/G snv 0.25
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
Diabetes Mellitus, Non-Insulin-Dependent 		0.810 1.000 4 2010 2014
dbSNP: rs1050828
rs1050828
G6PD
0.790 0.200 X 154536002 missense variant C/T snv 9.1E-03 3.6E-02
CUI: C4528257
Disease: Corpuscular Hemoglobin Concentration Mean
Corpuscular Hemoglobin Concentration Mean 		0.700 1.000 2 2013 2013
dbSNP: rs12393627
rs12393627
ARSL
X 2967682 intron variant A/G snv 0.11
CUI: C0489786
Disease: Height
Height 		0.700 1.000 2 2011 2012
dbSNP: rs1327301
rs1327301 		0.882 0.160 X 51467205 downstream gene variant C/T snv 0.29
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate 		0.700 1.000 2 2008 2009
dbSNP: rs13397
rs13397
TMEM187 ; MIR3202-2
0.925 0.200 X 153982797 synonymous variant G/A snv 0.27 0.15
CUI: C0007570
Disease: Celiac Disease
Celiac Disease 		0.800 1.000 2 2011 2012
dbSNP: rs2497938
rs2497938 		0.807 0.080 X 67343176 intergenic variant T/C snv 0.37
CUI: C4083212
Disease: Alopecia, Male Pattern
Alopecia, Male Pattern 		0.800 1.000 2 2011 2012
dbSNP: rs5945572
rs5945572 		0.882 0.160 X 51486831 downstream gene variant A/G snv
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate 		0.730 1.000 2 2008 2010
dbSNP: rs5984894
rs5984894
PCDH11X
0.925 0.080 X 92138738 intron variant A/G snv 0.54
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease 		0.700 1.000 2 2009 2011
dbSNP: rs1011526
rs1011526
HEPH
1.000 0.080 X 66196245 intron variant G/A snv 0.41
CUI: C4083212
Disease: Alopecia, Male Pattern
Alopecia, Male Pattern 		0.700 1.000 1 2012 2012
dbSNP: rs10127016
rs10127016
KANTR
1.000 0.040 X 53122914 intron variant G/T snv
CUI: C0009447
Disease: Common Variable Immunodeficiency
Common Variable Immunodeficiency 		0.700 1.000 1 2011 2011
dbSNP: rs1027970
rs1027970 		1.000 0.080 X 67155295 intergenic variant C/T snv 0.64
CUI: C4083212
Disease: Alopecia, Male Pattern
Alopecia, Male Pattern 		0.700 1.000 1 2012 2012
dbSNP: rs1041668
rs1041668 		1.000 0.080 X 66866114 intergenic variant G/A;C snv
CUI: C4083212
Disease: Alopecia, Male Pattern
Alopecia, Male Pattern 		0.700 1.000 1 2012 2012
dbSNP: rs1091486
rs1091486
HEPH
1.000 0.080 X 66219622 intron variant C/T snv 0.30
CUI: C4083212
Disease: Alopecia, Male Pattern
Alopecia, Male Pattern 		0.700 1.000 1 2012 2012
dbSNP: rs11094062
rs11094062 		1.000 0.080 X 67968686 intergenic variant A/G snv 0.46
CUI: C4083212
Disease: Alopecia, Male Pattern
Alopecia, Male Pattern 		0.700 1.000 1 2012 2012
dbSNP: rs11095197
rs11095197
TAB3
1.000 0.040 X 30958830 intron variant C/T snv 0.28
CUI: C0009447
Disease: Common Variable Immunodeficiency
Common Variable Immunodeficiency 		0.700 1.000 1 2011 2011
dbSNP: rs111705907
rs111705907
ARHGEF6
X 136761844 intron variant A/G snv 1.1E-02
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2012 2012
dbSNP: rs12007229
rs12007229 		1.000 0.120 X 67528513 upstream gene variant C/A snv 0.11
CUI: C0011269
Disease: Dementia, Vascular
Dementia, Vascular 		0.700 1.000 1 2012 2012
dbSNP: rs12007727
rs12007727 		1.000 0.080 X 67185587 intergenic variant G/A snv 0.11
CUI: C4083212
Disease: Alopecia, Male Pattern
Alopecia, Male Pattern 		0.700 1.000 1 2012 2012
dbSNP: rs12008279
rs12008279
CLDN2 ; MORC4
0.882 0.080 X 106917472 intron variant A/G;T snv
CUI: C0030305
Disease: Pancreatitis
Pancreatitis 		0.700 1.000 1 2012 2012
dbSNP: rs12008699
rs12008699 		1.000 0.080 X 68031571 intergenic variant G/A snv 0.19
CUI: C4083212
Disease: Alopecia, Male Pattern
Alopecia, Male Pattern 		0.700 1.000 1 2012 2012
dbSNP: rs12009526
rs12009526 		1.000 0.080 X 67983092 intergenic variant G/A snv 0.24
CUI: C4083212
Disease: Alopecia, Male Pattern
Alopecia, Male Pattern 		0.700 1.000 1 2012 2012
dbSNP: rs12009759
rs12009759 		1.000 0.080 X 67229645 intergenic variant G/A snv 9.0E-02
CUI: C4083212
Disease: Alopecia, Male Pattern
Alopecia, Male Pattern 		0.700 1.000 1 2012 2012
dbSNP: rs12010175
rs12010175
CCNQ
1.000 0.080 X 153597180 intron variant A/G snv
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
Diabetes Mellitus, Non-Insulin-Dependent 		0.800 1.000 1 2013 2013