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: rs1278352
rs1278352
ADAM12
1.000 0.040 10 126084807 intron variant A/G snv 0.61
CUI: C1263846
Disease: Attention deficit hyperactivity disorder
Attention deficit hyperactivity disorder 		0.700 1.000 2 2016 2016
dbSNP: rs10794057
rs10794057
ADAM12
10 126041165 intron variant T/C snv 0.44
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement 		0.700 1.000 1 2018 2018
dbSNP: rs10901553
rs10901553
ADAM12
10 126180175 intron variant A/G snv 0.31
CUI: C0040420
Disease: Tonometry
Tonometry 		0.700 1.000 1 2018 2018
dbSNP: rs1278259
rs1278259
ADAM12
10 126042533 intron variant A/G snv 0.70
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs1676712
rs1676712
ADAM12
1.000 0.080 10 126148271 intron variant A/G snv 0.10
CUI: C2076600
Disease: Influenza due to Influenza A virus subtype H1N1
Influenza due to Influenza A virus subtype H1N1 		0.700 1.000 1 2015 2015
dbSNP: rs35025137
rs35025137
ADAM12
10 126101214 missense variant C/T snv 5.6E-05 4.9E-05
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement 		0.700 1.000 1 2012 2012
dbSNP: rs4962322
rs4962322
ADAM12
10 126244196 intron variant C/A snv 0.13
CUI: C0021704
Disease: Intelligence
Intelligence 		0.700 1.000 1 2018 2018
dbSNP: rs4962336
rs4962336
ADAM12
10 126292592 intron variant T/C snv 0.28
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs7084390
rs7084390
ADAM12
10 126073189 intron variant A/G snv 0.18
CUI: C4528257
Disease: Corpuscular Hemoglobin Concentration Mean
Corpuscular Hemoglobin Concentration Mean 		0.700 1.000 1 2012 2012
dbSNP: rs1459457663
rs1459457663
ADAM12
1.000 0.080 10 126064988 missense variant C/T snv
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast 		0.700 0
dbSNP: rs151030407
rs151030407
ADAM12
1.000 0.080 10 126017332 missense variant G/A;C snv 5.0E-05 4.9E-05
CUI: C1321872
Disease: Stage IV Skin Melanoma
Stage IV Skin Melanoma 		0.700 0
dbSNP: rs3740199
rs3740199
ADAM12
0.882 0.120 10 126330456 missense variant C/A;G snv 2.1E-03; 0.56
CUI: C0409959
Disease: Osteoarthritis, Knee
Osteoarthritis, Knee 		0.050 0.600 5 2012 2017
dbSNP: rs1871054
rs1871054
ADAM12
0.925 0.040 10 126093840 intron variant C/A;T snv
CUI: C0029408
Disease: Degenerative polyarthritis
Degenerative polyarthritis 		0.040 0.750 4 2009 2017
dbSNP: rs1044122
rs1044122
ADAM12
0.925 0.040 10 126036209 synonymous variant A/G snv 0.27 0.26
CUI: C0409959
Disease: Osteoarthritis, Knee
Osteoarthritis, Knee 		0.030 0.667 3 2014 2017
dbSNP: rs3740199
rs3740199
ADAM12
0.882 0.120 10 126330456 missense variant C/A;G snv 2.1E-03; 0.56
CUI: C0029408
Disease: Degenerative polyarthritis
Degenerative polyarthritis 		0.030 1.000 3 2009 2017
dbSNP: rs1871054
rs1871054
ADAM12
0.925 0.040 10 126093840 intron variant C/A;T snv
CUI: C0409959
Disease: Osteoarthritis, Knee
Osteoarthritis, Knee 		0.020 0.500 2 2017 2017
dbSNP: rs1044122
rs1044122
ADAM12
0.925 0.040 10 126036209 synonymous variant A/G snv 0.27 0.26
CUI: C0029408
Disease: Degenerative polyarthritis
Degenerative polyarthritis 		0.010 1.000 1 2017 2017
dbSNP: rs11244787
rs11244787
ADAM12
1.000 0.080 10 126046147 intron variant A/G snv 0.13 0.13
CUI: C0275544
Disease: Congenital infectious disease
Congenital infectious disease 		0.010 1.000 1 2016 2016
dbSNP: rs11244787
rs11244787
ADAM12
1.000 0.080 10 126046147 intron variant A/G snv 0.13 0.13
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease 		0.010 1.000 1 2010 2010
dbSNP: rs1278279
rs1278279
ADAM12
0.925 0.040 10 126064909 missense variant G/A;C snv 0.27
CUI: C0029408
Disease: Degenerative polyarthritis
Degenerative polyarthritis 		0.010 < 0.001 1 2017 2017
dbSNP: rs1278279
rs1278279
ADAM12
0.925 0.040 10 126064909 missense variant G/A;C snv 0.27
CUI: C0409959
Disease: Osteoarthritis, Knee
Osteoarthritis, Knee 		0.010 < 0.001 1 2017 2017
dbSNP: rs1278300
rs1278300
ADAM12
1.000 0.040 10 126102615 intron variant A/G;T snv
CUI: C2745963
Disease: Kashin-Beck Disease
Kashin-Beck Disease 		0.010 1.000 1 2016 2016
dbSNP: rs1710286
rs1710286
ADAM12
0.925 0.080 10 126052599 intron variant C/G snv 0.54
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma 		0.010 1.000 1 2017 2017
dbSNP: rs1710286
rs1710286
ADAM12
0.925 0.080 10 126052599 intron variant C/G snv 0.54
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast 		0.010 1.000 1 2017 2017
dbSNP: rs1871054
rs1871054
ADAM12
0.925 0.040 10 126093840 intron variant C/A;T snv
CUI: C0275544
Disease: Congenital infectious disease
Congenital infectious disease 		0.010 1.000 1 2016 2016