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: rs12780845
rs12780845
TRDMT1
10 17181245 intron variant A/G snv 0.34
CUI: C2242817
Disease: Homocysteine measurement
Homocysteine measurement 		0.800 1.000 1 2013 2013
dbSNP: rs17381591
rs17381591
TRDMT1
1.000 0.080 10 17202049 non coding transcript exon variant T/C snv 0.28
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction 		0.700 1.000 1 2011 2011
dbSNP: rs3780962
rs3780962
TRDMT1
10 17151347 intron variant A/G snv 0.52
CUI: C0427460
Disease: Red cell distribution width determination
Red cell distribution width determination 		0.700 1.000 1 2019 2019
dbSNP: rs3780962
rs3780962
TRDMT1
10 17151347 intron variant A/G snv 0.52
CUI: C1304746
Disease: RDW - Red blood cell distribution width result
RDW - Red blood cell distribution width result 		0.700 1.000 1 2019 2019
dbSNP: rs7901017
rs7901017
TRDMT1
10 17192393 intron variant T/C snv 6.8E-02
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.700 1.000 1 2012 2012
dbSNP: rs7901017
rs7901017
TRDMT1
10 17192393 intron variant T/C snv 6.8E-02
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement 		0.700 1.000 1 2012 2012
dbSNP: rs11254413
rs11254413
TRDMT1
0.851 0.120 10 17162188 missense variant G/A snv 0.41 0.44
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma 		0.010 1.000 1 2012 2012
dbSNP: rs11254413
rs11254413
TRDMT1
0.851 0.120 10 17162188 missense variant G/A snv 0.41 0.44
CUI: C0024623
Disease: Malignant neoplasm of stomach
Malignant neoplasm of stomach 		0.010 1.000 1 2012 2012
dbSNP: rs11254413
rs11254413
TRDMT1
0.851 0.120 10 17162188 missense variant G/A snv 0.41 0.44
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast 		0.010 1.000 1 2012 2012
dbSNP: rs11254413
rs11254413
TRDMT1
0.851 0.120 10 17162188 missense variant G/A snv 0.41 0.44
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma 		0.010 1.000 1 2012 2012
dbSNP: rs6602178
rs6602178
TRDMT1
10 17138170 3 prime UTR variant A/C snv 0.51
CUI: C0018798
Disease: Congenital Heart Defects
Congenital Heart Defects 		0.010 1.000 1 2017 2017
dbSNP: rs7074891
rs7074891
TRDMT1
0.925 0.120 10 17146475 3 prime UTR variant C/T snv 0.95
CUI: C0235974
Disease: Pancreatic carcinoma
Pancreatic carcinoma 		0.010 1.000 1 2013 2013
dbSNP: rs7074891
rs7074891
TRDMT1
0.925 0.120 10 17146475 3 prime UTR variant C/T snv 0.95
CUI: C0346647
Disease: Malignant neoplasm of pancreas
Malignant neoplasm of pancreas 		0.010 1.000 1 2013 2013