Source: ALL

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs786205050
rs786205050
CACNA1H
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease 		G 0.710 CausalMutation CLINVAR

dbSNP: rs867593888
rs867593888
MYH9
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease 		C 0.700 GeneticVariation CLINVAR

dbSNP: rs758379595
rs758379595
CLCN2
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease 		T 0.700 CausalMutation CLINVAR

dbSNP: rs587777449
rs587777449
IFIH1
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease 		A 0.700 GeneticVariation CLINVAR

dbSNP: rs569681869
rs569681869
COL4A4
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease 		G 0.700 GeneticVariation CLINVAR

dbSNP: rs533297350
rs533297350
COL4A4
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease 		T 0.700 GeneticVariation CLINVAR

dbSNP: rs530391015
rs530391015
INF2
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease 		A 0.700 GeneticVariation CLINVAR

dbSNP: rs312262690
rs312262690
ANTXR2
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease 		AG 0.700 CausalMutation CLINVAR

dbSNP: rs281874674
rs281874674
COL4A5
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease 		C 0.700 GeneticVariation CLINVAR

dbSNP: rs2230288
rs2230288
GBA
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease 		T 0.700 SusceptibilityMutation CLINVAR

dbSNP: rs1557551678
rs1557551678
CLDN19
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease 		A 0.700 CausalMutation CLINVAR

dbSNP: rs1555206402
rs1555206402
HMBS
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease 		A 0.700 CausalMutation CLINVAR

dbSNP: rs1553857113
rs1553857113
CLCN2
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease 		T 0.700 CausalMutation CLINVAR

dbSNP: rs1553856214
rs1553856214
CLCN2
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease 		A 0.700 CausalMutation CLINVAR

dbSNP: rs1553853557
rs1553853557
CLCN2 ; FAM131A
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease 		G 0.700 CausalMutation CLINVAR

dbSNP: rs1553201258
rs1553201258
DARS2
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease 		C 0.700 CausalMutation CLINVAR

dbSNP: rs148636776
rs148636776
ATXN2 ; SH2B3
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease 		A 0.700 CausalMutation CLINVAR

dbSNP: rs142433332
rs142433332
DARS2
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease 		C 0.700 CausalMutation CLINVAR

dbSNP: rs141498002
rs141498002
PMM2
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease 		A 0.700 GeneticVariation CLINVAR

dbSNP: rs1293789661
rs1293789661
CLCN2
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease 		T 0.700 CausalMutation CLINVAR

dbSNP: rs118204456
rs118204456
F12 ; GRK6 ; SLC34A1
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease 		C 0.700 CausalMutation CLINVAR

dbSNP: rs1057523354
rs1057523354
COL4A1
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease 		A 0.700 CausalMutation CLINVAR

dbSNP: rs1057518959
rs1057518959
PKD1 ; MIR1225 ; LOC105371049
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease 		G 0.700 GeneticVariation CLINVAR

dbSNP: rs1057518903
rs1057518903
MEN1
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease 		A 0.700 CausalMutation CLINVAR

dbSNP: rs1057518899
rs1057518899
PKD1
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease 		A 0.700 CausalMutation CLINVAR