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: rs1250550
rs1250550
0.851 0.240 10 79300560 intron variant C/A snv 0.27
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
0.820 1.000 1 2010 2017
dbSNP: rs12571751
rs12571751
0.925 0.120 10 79182874 intron variant A/G snv 0.46
Diabetes Mellitus, Non-Insulin-Dependent
0.810 0.750 2 2012 2017
dbSNP: rs1250544
rs1250544
0.882 0.080 10 79273128 intron variant G/A snv 0.32
CUI: C0033860
Disease: Psoriasis
Psoriasis
0.810 1.000 1 2012 2012
dbSNP: rs1250550
rs1250550
0.851 0.240 10 79300560 intron variant C/A snv 0.27
CUI: C0021390
Disease: Inflammatory Bowel Diseases
Inflammatory Bowel Diseases
0.810 1.000 1 2009 2017
dbSNP: rs1250550
rs1250550
0.851 0.240 10 79300560 intron variant C/A snv 0.27
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis
0.800 1.000 2 2011 2019
dbSNP: rs1250552
rs1250552
0.882 0.200 10 79298270 intron variant A/C;G snv
CUI: C0007570
Disease: Celiac Disease
Celiac Disease
0.800 1.000 2 2010 2011
dbSNP: rs11593576
rs11593576
0.925 0.040 10 79256139 intron variant C/T snv 0.29
CUI: C0042900
Disease: Vitiligo
Vitiligo
0.800 1.000 1 2010 2010
dbSNP: rs1250542
rs1250542
1.000 0.080 10 79274913 intron variant G/A snv 0.32
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis
0.800 1.000 1 2011 2011
dbSNP: rs1250546
rs1250546
0.925 0.080 10 79272775 intron variant A/G snv 0.36
CUI: C0021390
Disease: Inflammatory Bowel Diseases
Inflammatory Bowel Diseases
0.800 1.000 1 2012 2012
dbSNP: rs1250546
rs1250546
0.925 0.080 10 79272775 intron variant A/G snv 0.36
CUI: C0033860
Disease: Psoriasis
Psoriasis
0.800 1.000 1 2012 2012
dbSNP: rs704010
rs704010
0.851 0.080 10 79081391 intron variant T/C snv 0.71
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast
0.720 1.000 2 2010 2016
dbSNP: rs1250552
rs1250552
0.882 0.200 10 79298270 intron variant A/C;G snv
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis
0.700 1.000 1 2011 2011
dbSNP: rs1250552
rs1250552
0.882 0.200 10 79298270 intron variant A/C;G snv
CUI: C0021053
Disease: Immune System Diseases
Immune System Diseases
0.700 1.000 1 2011 2011
dbSNP: rs1250552
rs1250552
0.882 0.200 10 79298270 intron variant A/C;G snv
CUI: C0004364
Disease: Autoimmune Diseases
Autoimmune Diseases
0.700 1.000 1 2011 2011
dbSNP: rs1250552
rs1250552
0.882 0.200 10 79298270 intron variant A/C;G snv
CUI: C0004096
Disease: Asthma
Asthma
0.700 1.000 1 2011 2011
dbSNP: rs1749824
rs1749824
0.925 0.080 10 79164105 intron variant C/A snv 0.39
CUI: C0025303
Disease: Meningococcal Infections
Meningococcal Infections
0.700 1.000 1 2010 2010
dbSNP: rs780151
rs780151
10 79171724 intron variant G/A snv 0.32
CUI: C0489786
Disease: Height
Height
0.700 1.000 1 2013 2013
dbSNP: rs7916441
rs7916441
10 79165820 intron variant G/C snv 0.39
CUI: C0489786
Disease: Height
Height
0.700 1.000 1 2010 2010