Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs11591741
rs11591741
1.000 0.080 10 100216744 intron variant G/C snv 0.30
Diabetes Mellitus, Non-Insulin-Dependent
Nutritional and Metabolic Diseases; Endocrine System Diseases 0.700 1.000 1 2018 2018
dbSNP: rs11597086
rs11597086
10 100193948 non coding transcript exon variant A/C snv 0.30 0.29
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.700 1.000 1 2012 2012
dbSNP: rs17882802
rs17882802
10 100223656 intron variant G/A snv 0.30
CUI: C1629609
Disease: Age at menopause
Age at menopause
0.700 1.000 1 2019 2019
dbSNP: rs17883880
rs17883880
10 100230590 intron variant T/A snv 1.2E-02
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.700 1.000 1 2012 2012
dbSNP: rs17883880
rs17883880
10 100230590 intron variant T/A snv 1.2E-02
CUI: C0428474
Disease: Serum LDL cholesterol measurement
Serum LDL cholesterol measurement
0.700 1.000 1 2012 2012
dbSNP: rs17883880
rs17883880
10 100230590 intron variant T/A snv 1.2E-02
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.700 1.000 1 2012 2012
dbSNP: rs17883880
rs17883880
10 100230590 intron variant T/A snv 1.2E-02
Low density lipoprotein cholesterol measurement
0.700 1.000 1 2012 2012
dbSNP: rs267606736
rs267606736
1.000 10 100205167 stop gained G/A snv 1.2E-05 2.1E-05
CUI: C3150891
Disease: COCOON SYNDROME
COCOON SYNDROME
0.700 0
dbSNP: rs2230804
rs2230804
10 100218126 missense variant C/T snv 0.47 0.57
CUI: C0043144
Disease: Wheezing
Wheezing
Pathological Conditions, Signs and Symptoms 0.010 1.000 1 2014 2014