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: rs387906894
rs387906894
CORIN
1.000 4 47683803 missense variant T/C snv 4.0E-06
CUI: C3281288
Disease: PREECLAMPSIA/ECLAMPSIA 5
PREECLAMPSIA/ECLAMPSIA 5 		0.800 1.000 1 2012 2012
dbSNP: rs387906895
rs387906895
CORIN
1.000 4 47665207 missense variant T/C snv
CUI: C3281288
Disease: PREECLAMPSIA/ECLAMPSIA 5
PREECLAMPSIA/ECLAMPSIA 5 		0.800 1.000 1 2012 2012
dbSNP: rs16860432
rs16860432
CORIN
4 47598898 intron variant G/C snv 4.6E-02
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.700 1.000 1 2012 2012
dbSNP: rs16860432
rs16860432
CORIN
4 47598898 intron variant G/C snv 4.6E-02
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement 		0.700 1.000 1 2012 2012
dbSNP: rs16860535
rs16860535
CORIN
4 47673673 intron variant G/A;C snv 3.0E-02
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.700 1.000 1 2012 2012
dbSNP: rs16860535
rs16860535
CORIN
4 47673673 intron variant G/A;C snv 3.0E-02
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement 		0.700 1.000 1 2012 2012
dbSNP: rs4695266
rs4695266
CORIN
4 47670263 intron variant T/A;C snv
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.700 1.000 1 2012 2012
dbSNP: rs4695266
rs4695266
CORIN
4 47670263 intron variant T/A;C snv
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.700 1.000 1 2012 2012
dbSNP: rs4695266
rs4695266
CORIN
4 47670263 intron variant T/A;C snv
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement 		0.700 1.000 1 2012 2012
dbSNP: rs111253292
rs111253292
CORIN
4 47661743 missense variant T/G snv 4.6E-03 2.0E-02
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease 		0.030 1.000 3 2007 2012
dbSNP: rs75770792
rs75770792
CORIN
4 47661782 missense variant G/A snv 4.6E-03 2.0E-02
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease 		0.030 1.000 3 2007 2012
dbSNP: rs2271037
rs2271037
CORIN
4 47678068 intron variant T/C;G snv 4.0E-06; 0.30
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease 		0.010 1.000 1 2018 2018
dbSNP: rs3749585
rs3749585
CORIN
4 47595573 3 prime UTR variant A/G snv 0.11
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease 		0.010 1.000 1 2018 2018