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: rs760761240
rs760761240
1.000 0.080 17 34256290 missense variant G/A;C snv 6.0E-05
CUI: C0155626
Disease: Acute myocardial infarction
Acute myocardial infarction
0.010 1.000 1 2007 2007
dbSNP: rs2857657
rs2857657
1.000 0.040 17 34256113 non coding transcript exon variant G/C snv 0.86
CUI: C0409959
Disease: Osteoarthritis, Knee
Osteoarthritis, Knee
0.010 1.000 1 2013 2013
dbSNP: rs3917887
rs3917887
0.776 0.240 17 34255979 non coding transcript exon variant AGCTCCTCCTTCTC/-;AGCTCCTCCTTCTCAGCTCCTCCTTCTC delins 0.33
Malignant neoplasm of urinary bladder
0.010 1.000 1 2012 2012
dbSNP: rs3917887
rs3917887
0.776 0.240 17 34255979 non coding transcript exon variant AGCTCCTCCTTCTC/-;AGCTCCTCCTTCTCAGCTCCTCCTTCTC delins 0.33
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate
0.010 1.000 1 2015 2015
dbSNP: rs3917887
rs3917887
0.776 0.240 17 34255979 non coding transcript exon variant AGCTCCTCCTTCTC/-;AGCTCCTCCTTCTCAGCTCCTCCTTCTC delins 0.33
CUI: C0005695
Disease: Bladder Neoplasm
Bladder Neoplasm
0.010 1.000 1 2012 2012
dbSNP: rs3917887
rs3917887
0.776 0.240 17 34255979 non coding transcript exon variant AGCTCCTCCTTCTC/-;AGCTCCTCCTTCTCAGCTCCTCCTTCTC delins 0.33
CUI: C0022661
Disease: Kidney Failure, Chronic
Kidney Failure, Chronic
0.010 1.000 1 2014 2014
dbSNP: rs3917887
rs3917887
0.776 0.240 17 34255979 non coding transcript exon variant AGCTCCTCCTTCTC/-;AGCTCCTCCTTCTCAGCTCCTCCTTCTC delins 0.33
CUI: C0011881
Disease: Diabetic Nephropathy
Diabetic Nephropathy
0.010 1.000 1 2014 2014
dbSNP: rs3917887
rs3917887
0.776 0.240 17 34255979 non coding transcript exon variant AGCTCCTCCTTCTC/-;AGCTCCTCCTTCTCAGCTCCTCCTTCTC delins 0.33
CUI: C0041330
Disease: Tuberculosis, Spinal
Tuberculosis, Spinal
0.010 1.000 1 2016 2016
dbSNP: rs3917887
rs3917887
0.776 0.240 17 34255979 non coding transcript exon variant AGCTCCTCCTTCTC/-;AGCTCCTCCTTCTCAGCTCCTCCTTCTC delins 0.33
CUI: C0600139
Disease: Prostate carcinoma
Prostate carcinoma
0.010 1.000 1 2015 2015
dbSNP: rs3917887
rs3917887
0.776 0.240 17 34255979 non coding transcript exon variant AGCTCCTCCTTCTC/-;AGCTCCTCCTTCTCAGCTCCTCCTTCTC delins 0.33
CUI: C0699885
Disease: Carcinoma of bladder
Carcinoma of bladder
0.010 1.000 1 2012 2012
dbSNP: rs746076530
rs746076530
1.000 0.080 17 34256238 synonymous variant A/G snv 1.6E-05 7.0E-06
CUI: C0002736
Disease: Amyotrophic Lateral Sclerosis
Amyotrophic Lateral Sclerosis
0.040 1.000 4 2011 2014
dbSNP: rs4586
rs4586
0.790 0.280 17 34256250 synonymous variant T/C snv 0.44 0.48
CUI: C0242383
Disease: Age related macular degeneration
Age related macular degeneration
0.020 1.000 2 2013 2018
dbSNP: rs4586
rs4586
0.790 0.280 17 34256250 synonymous variant T/C snv 0.44 0.48
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.010 1.000 1 2016 2016
dbSNP: rs4586
rs4586
0.790 0.280 17 34256250 synonymous variant T/C snv 0.44 0.48
CUI: C0085207
Disease: Gestational Diabetes
Gestational Diabetes
0.010 < 0.001 1 2017 2017
dbSNP: rs4586
rs4586
0.790 0.280 17 34256250 synonymous variant T/C snv 0.44 0.48
CUI: C0409959
Disease: Osteoarthritis, Knee
Osteoarthritis, Knee
0.010 1.000 1 2007 2007
dbSNP: rs4586
rs4586
0.790 0.280 17 34256250 synonymous variant T/C snv 0.44 0.48
CUI: C0029408
Disease: Degenerative polyarthritis
Degenerative polyarthritis
0.010 1.000 1 2019 2019
dbSNP: rs4586
rs4586
0.790 0.280 17 34256250 synonymous variant T/C snv 0.44 0.48
CUI: C0041296
Disease: Tuberculosis
Tuberculosis
0.010 1.000 1 2011 2011
dbSNP: rs4586
rs4586
0.790 0.280 17 34256250 synonymous variant T/C snv 0.44 0.48
CUI: C0022661
Disease: Kidney Failure, Chronic
Kidney Failure, Chronic
0.010 1.000 1 2012 2012
dbSNP: rs4586
rs4586
0.790 0.280 17 34256250 synonymous variant T/C snv 0.44 0.48
CUI: C2316810
Disease: Chronic kidney disease stage 5
Chronic kidney disease stage 5
0.010 1.000 1 2012 2012
dbSNP: rs13900
rs13900
0.925 0.120 17 34256892 3 prime UTR variant C/T snv 0.28
CUI: C0019196
Disease: Hepatitis C
Hepatitis C
0.010 1.000 1 2019 2019
dbSNP: rs13900
rs13900
0.925 0.120 17 34256892 3 prime UTR variant C/T snv 0.28
CUI: C0023283
Disease: Leishmaniasis, Cutaneous
Leishmaniasis, Cutaneous
0.010 1.000 1 2020 2020
dbSNP: rs2857656
rs2857656
0.851 0.120 17 34254988 upstream gene variant G/A;C snv
CUI: C0041330
Disease: Tuberculosis, Spinal
Tuberculosis, Spinal
0.020 1.000 2 2014 2016
dbSNP: rs3760396
rs3760396
0.732 0.280 17 34254422 upstream gene variant G/C snv 0.15
CUI: C0007131
Disease: Non-Small Cell Lung Carcinoma
Non-Small Cell Lung Carcinoma
0.020 1.000 2 2011 2016
dbSNP: rs2857656
rs2857656
0.851 0.120 17 34254988 upstream gene variant G/A;C snv
CUI: C0243026
Disease: Sepsis
Sepsis
0.010 1.000 1 2017 2017
dbSNP: rs2857656
rs2857656
0.851 0.120 17 34254988 upstream gene variant G/A;C snv
CUI: C0036690
Disease: Septicemia
Septicemia
0.010 1.000 1 2017 2017