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: rs780159
rs780159
10 79147390 intron variant A/C;G snv
CUI: C0205682
Disease: Waist-Hip Ratio
Waist-Hip Ratio
0.700 1.000 2 2018 2019
dbSNP: rs7916441
rs7916441
10 79165820 intron variant G/C snv 0.39
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 2 2010 2019
dbSNP: rs1250566
rs1250566
10 79286696 intron variant G/A snv 0.24
CUI: C0021390
Disease: Inflammatory Bowel Diseases
Inflammatory Bowel Diseases
0.700 1.000 1 2015 2015
dbSNP: rs1658319
rs1658319
10 79165257 intron variant T/C snv 0.81
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 1 2019 2019
dbSNP: rs1815314
rs1815314
10 79169036 intron variant G/A;C;T snv
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 1 2014 2014
dbSNP: rs2802372
rs2802372
10 79287818 intron variant A/C snv 0.44
CUI: C0857490
Disease: Granulocyte count
Granulocyte count
0.700 1.000 1 2016 2016
dbSNP: rs703984
rs703984
10 79181660 intron variant G/C;T snv
CUI: C0205682
Disease: Waist-Hip Ratio
Waist-Hip Ratio
0.700 1.000 1 2019 2019
dbSNP: rs74142329
rs74142329
10 79190231 intron variant C/T snv 4.9E-02
Platelet Component Distribution Width Measurement
0.700 1.000 1 2016 2016
dbSNP: rs779933
rs779933
10 79158760 intron variant G/A snv 0.36
CUI: C0205682
Disease: Waist-Hip Ratio
Waist-Hip Ratio
0.700 1.000 1 2019 2019
dbSNP: rs779933
rs779933
10 79158760 intron variant G/A snv 0.36
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 1 2015 2015
dbSNP: rs780151
rs780151
10 79171724 intron variant G/A snv 0.32
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 1 2013 2013
dbSNP: rs780159
rs780159
10 79147390 intron variant A/C;G snv
CUI: C4049938
Disease: Physical Activity Measurement
Physical Activity Measurement
0.700 1.000 1 2017 2017
dbSNP: rs7914926
rs7914926
10 79170941 intron variant A/G snv 0.41
CUI: C0042834
Disease: Vital capacity
Vital capacity
0.700 1.000 1 2017 2017
dbSNP: rs7916441
rs7916441
10 79165820 intron variant G/C snv 0.39
CUI: C0042834
Disease: Vital capacity
Vital capacity
0.700 1.000 1 2019 2019
dbSNP: rs11593576
rs11593576
0.925 0.040 10 79256139 intron variant C/T snv 0.29
CUI: C0033860
Disease: Psoriasis
Psoriasis
0.700 1.000 1 2015 2015
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: rs1250569
rs1250569
0.925 0.040 10 79285450 intron variant T/C snv 0.44 0.51
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
0.720 1.000 1 2015 2017
dbSNP: rs704010
rs704010
0.851 0.080 10 79081391 intron variant T/C snv 0.71
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma
0.720 1.000 4 2010 2017
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: rs1250544
rs1250544
0.882 0.080 10 79273128 intron variant G/A snv 0.32
CUI: C0263361
Disease: Psoriasis vulgaris
Psoriasis vulgaris
0.700 1.000 1 2015 2015
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: rs1250544
rs1250544
0.882 0.080 10 79273128 intron variant G/A snv 0.32
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
0.700 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: rs1250546
rs1250546
0.925 0.080 10 79272775 intron variant A/G snv 0.36
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
0.700 1.000 1 2015 2015
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