Source: BEFREE

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: rs10774671
rs10774671
0.732 0.480 12 112919388 splice acceptor variant G/A;C snv 0.67
Diabetes Mellitus, Insulin-Dependent
0.030 0.667 3 2006 2009
dbSNP: rs10774671
rs10774671
0.732 0.480 12 112919388 splice acceptor variant G/A;C snv 0.67
CUI: C1527336
Disease: Sjogren's Syndrome
Sjogren's Syndrome
0.020 1.000 2 2017 2017
dbSNP: rs10774671
rs10774671
0.732 0.480 12 112919388 splice acceptor variant G/A;C snv 0.67
CUI: C0019196
Disease: Hepatitis C
Hepatitis C
0.020 1.000 2 2013 2015
dbSNP: rs3741981
rs3741981
0.882 0.120 12 112911065 missense variant G/A;C snv
CUI: C0019196
Disease: Hepatitis C
Hepatitis C
0.020 1.000 2 2013 2015
dbSNP: rs10774671
rs10774671
0.732 0.480 12 112919388 splice acceptor variant G/A;C snv 0.67
CUI: C0041296
Disease: Tuberculosis
Tuberculosis
0.010 1.000 1 2018 2018
dbSNP: rs10774671
rs10774671
0.732 0.480 12 112919388 splice acceptor variant G/A;C snv 0.67
CUI: C0019163
Disease: Hepatitis B
Hepatitis B
0.010 1.000 1 2017 2017
dbSNP: rs10774671
rs10774671
0.732 0.480 12 112919388 splice acceptor variant G/A;C snv 0.67
CUI: C0008055
Disease: Chikungunya Fever
Chikungunya Fever
0.010 1.000 1 2016 2016
dbSNP: rs10774671
rs10774671
0.732 0.480 12 112919388 splice acceptor variant G/A;C snv 0.67
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis
0.010 1.000 1 2012 2012
dbSNP: rs10774671
rs10774671
0.732 0.480 12 112919388 splice acceptor variant G/A;C snv 0.67
CUI: C0275524
Disease: Coinfection
Coinfection
0.010 1.000 1 2016 2016
dbSNP: rs10774671
rs10774671
0.732 0.480 12 112919388 splice acceptor variant G/A;C snv 0.67
CUI: C2239176
Disease: Liver carcinoma
Liver carcinoma
0.010 < 0.001 1 2016 2016
dbSNP: rs10774671
rs10774671
0.732 0.480 12 112919388 splice acceptor variant G/A;C snv 0.67
CUI: C0239946
Disease: Fibrosis, Liver
Fibrosis, Liver
0.010 1.000 1 2015 2015
dbSNP: rs10774671
rs10774671
0.732 0.480 12 112919388 splice acceptor variant G/A;C snv 0.67
CUI: C1096184
Disease: West Nile viral infection
West Nile viral infection
0.010 1.000 1 2009 2009
dbSNP: rs10774671
rs10774671
0.732 0.480 12 112919388 splice acceptor variant G/A;C snv 0.67
CUI: C0042769
Disease: Virus Diseases
Virus Diseases
0.010 1.000 1 2017 2017
dbSNP: rs10774671
rs10774671
0.732 0.480 12 112919388 splice acceptor variant G/A;C snv 0.67
CUI: C0011311
Disease: Dengue Fever
Dengue Fever
0.010 < 0.001 1 2013 2013
dbSNP: rs10774671
rs10774671
0.732 0.480 12 112919388 splice acceptor variant G/A;C snv 0.67
CUI: C0018572
Disease: Hand, Foot and Mouth Disease
Hand, Foot and Mouth Disease
0.010 1.000 1 2014 2014
dbSNP: rs1131454
rs1131454
0.882 0.040 12 112911065 missense variant G/A;C snv 0.57
CUI: C0008055
Disease: Chikungunya Fever
Chikungunya Fever
0.010 1.000 1 2016 2016
dbSNP: rs1131454
rs1131454
0.882 0.040 12 112911065 missense variant G/A;C snv 0.57
CUI: C0011311
Disease: Dengue Fever
Dengue Fever
0.010 < 0.001 1 2013 2013
dbSNP: rs1131454
rs1131454
0.882 0.040 12 112911065 missense variant G/A;C snv 0.57
CUI: C0041296
Disease: Tuberculosis
Tuberculosis
0.010 1.000 1 2018 2018
dbSNP: rs11352835
rs11352835
1.000 0.080 12 112931911 frameshift variant A/- del 0.74
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis
0.010 1.000 1 2012 2012
dbSNP: rs2240190
rs2240190
1.000 0.040 12 112908322 intron variant C/A snv 4.9E-02
CUI: C0041296
Disease: Tuberculosis
Tuberculosis
0.010 1.000 1 2018 2018
dbSNP: rs2660
rs2660
0.851 0.160 12 112919637 missense variant G/A snv 0.71 0.75
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate
0.010 1.000 1 2011 2011
dbSNP: rs2660
rs2660
0.851 0.160 12 112919637 missense variant G/A snv 0.71 0.75
CUI: C0035920
Disease: Rubella
Rubella
0.010 1.000 1 2010 2010
dbSNP: rs2660
rs2660
0.851 0.160 12 112919637 missense variant G/A snv 0.71 0.75
CUI: C0019196
Disease: Hepatitis C
Hepatitis C
0.010 1.000 1 2013 2013
dbSNP: rs2660
rs2660
0.851 0.160 12 112919637 missense variant G/A snv 0.71 0.75
CUI: C0600139
Disease: Prostate carcinoma
Prostate carcinoma
0.010 1.000 1 2011 2011
dbSNP: rs34137742
rs34137742
0.925 0.080 12 112910856 intron variant C/T snv 0.13
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate
0.010 1.000 1 2011 2011