Source: ALL

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: rs11171739
rs11171739
0.807 0.320 12 56076841 5 prime UTR variant C/T snv 0.49
CUI: C0004096
Disease: Asthma
Asthma
0.700 1.000 1 2018 2018
dbSNP: rs11171739
rs11171739
0.807 0.320 12 56076841 5 prime UTR variant C/T snv 0.49
CUI: C1527304
Disease: Allergic Reaction
Allergic Reaction
0.700 1.000 1 2018 2018
dbSNP: rs11171739
rs11171739
0.807 0.320 12 56076841 5 prime UTR variant C/T snv 0.49
CUI: C0200635
Disease: Lymphocyte Count measurement
Lymphocyte Count measurement
0.700 1.000 1 2012 2012
dbSNP: rs11171739
rs11171739
0.807 0.320 12 56076841 5 prime UTR variant C/T snv 0.49
CUI: C0596887
Disease: mathematical ability
mathematical ability
0.700 1.000 1 2018 2018
dbSNP: rs2271194
rs2271194
1.000 0.120 12 56083910 splice region variant A/T snv 0.63 0.53
CUI: C0032460
Disease: Polycystic Ovary Syndrome
Polycystic Ovary Syndrome
0.700 1.000 1 2018 2018
dbSNP: rs2292239
rs2292239
0.742 0.480 12 56088396 intron variant T/G snv 0.65
CUI: C0002171
Disease: Alopecia Areata
Alopecia Areata
0.700 1.000 1 2015 2015
dbSNP: rs2292239
rs2292239
0.742 0.480 12 56088396 intron variant T/G snv 0.65
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis
0.700 1.000 1 2011 2011
dbSNP: rs2292239
rs2292239
0.742 0.480 12 56088396 intron variant T/G snv 0.65
CUI: C1272321
Disease: Autoantibody measurement
Autoantibody measurement
0.700 1.000 1 2011 2011
dbSNP: rs2292239
rs2292239
0.742 0.480 12 56088396 intron variant T/G snv 0.65
CUI: C0032460
Disease: Polycystic Ovary Syndrome
Polycystic Ovary Syndrome
0.700 1.000 1 2012 2012
dbSNP: rs34379766
rs34379766
12 56080359 missense variant C/A;T snv 4.6E-06; 4.6E-06
CUI: C0162701
Disease: Polysomnography
Polysomnography
0.700 1.000 1 2012 2012
dbSNP: rs79335261
rs79335261
1.000 0.080 12 56103857 intron variant G/A;T snv
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease
0.700 1.000 1 2016 2016
dbSNP: rs877636
rs877636
1.000 0.120 12 56086799 intron variant G/A snv 0.61
CUI: C0021704
Disease: Intelligence
Intelligence
0.700 1.000 1 2015 2015
dbSNP: rs877636
rs877636
1.000 0.120 12 56086799 intron variant G/A snv 0.61
CUI: C0032460
Disease: Polycystic Ovary Syndrome
Polycystic Ovary Syndrome
0.700 1.000 1 2012 2012
dbSNP: rs931676601
rs931676601
12 56097196 missense variant A/G;T snv
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.700 1.000 1 2013 2013
dbSNP: rs1057519893
rs1057519893
0.790 0.160 12 56085070 missense variant G/A;T snv
CUI: C1335167
Disease: Ovarian Mucinous Adenocarcinoma
Ovarian Mucinous Adenocarcinoma
0.700 0
dbSNP: rs1057519803
rs1057519803
0.925 0.080 12 56088138 missense variant G/A snv
CUI: C4733095
Disease: HER2-negative breast cancer
HER2-negative breast cancer
0.010 1.000 1 2015 2015
dbSNP: rs1057519803
rs1057519803
0.925 0.080 12 56088138 missense variant G/A snv
Secondary malignant neoplasm of liver
0.010 1.000 1 2015 2015
dbSNP: rs1057519891
rs1057519891
0.851 0.160 12 56088557 missense variant G/A;T snv 4.0E-06
CUI: C0038356
Disease: Stomach Neoplasms
Stomach Neoplasms
0.010 1.000 1 2015 2015
dbSNP: rs11171739
rs11171739
0.807 0.320 12 56076841 5 prime UTR variant C/T snv 0.49
CUI: C0221056
Disease: Adult type dermatomyositis
Adult type dermatomyositis
0.010 1.000 1 2015 2015
dbSNP: rs11171739
rs11171739
0.807 0.320 12 56076841 5 prime UTR variant C/T snv 0.49
CUI: C0011849
Disease: Diabetes Mellitus
Diabetes Mellitus
0.010 1.000 1 2015 2015
dbSNP: rs11171739
rs11171739
0.807 0.320 12 56076841 5 prime UTR variant C/T snv 0.49
CUI: C0011633
Disease: Dermatomyositis
Dermatomyositis
0.010 1.000 1 2015 2015
dbSNP: rs11171739
rs11171739
0.807 0.320 12 56076841 5 prime UTR variant C/T snv 0.49
CUI: C3250443
Disease: MYOTONIC DYSTROPHY 1
MYOTONIC DYSTROPHY 1
0.010 1.000 1 2015 2015
dbSNP: rs11171739
rs11171739
0.807 0.320 12 56076841 5 prime UTR variant C/T snv 0.49
CUI: C0085655
Disease: Polymyositis
Polymyositis
0.010 1.000 1 2015 2015
dbSNP: rs2292239
rs2292239
0.742 0.480 12 56088396 intron variant T/G snv 0.65
CUI: C0011633
Disease: Dermatomyositis
Dermatomyositis
0.010 1.000 1 2015 2015
dbSNP: rs2292239
rs2292239
0.742 0.480 12 56088396 intron variant T/G snv 0.65
CUI: C0154830
Disease: Proliferative diabetic retinopathy
Proliferative diabetic retinopathy
0.010 1.000 1 2015 2015