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: rs11611246
rs11611246
WNK1
12 830314 intron variant G/T snv 0.19
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 4 2015 2019
dbSNP: rs10774463
rs10774463
WNK1
12 792399 intron variant G/A;C snv
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: rs10774463
rs10774463
WNK1
12 792399 intron variant G/A;C snv
CUI: C0427460
Disease: Red cell distribution width determination
Red cell distribution width determination 		0.700 1.000 1 2019 2019
dbSNP: rs11064560
rs11064560
WNK1
12 834787 intron variant G/T snv 0.63
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease 		0.010 1.000 1 2014 2014
dbSNP: rs11554421
rs11554421
WNK1
12 753986 missense variant G/A snv 0.12 9.8E-02
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease 		0.010 1.000 1 2011 2011
dbSNP: rs11613704
rs11613704
WNK1
12 871759 intron variant C/A;T snv
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure 		0.700 1.000 1 2016 2016
dbSNP: rs11885
rs11885
WNK1
12 753919 missense variant G/A;T snv
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease 		0.010 1.000 1 2011 2011
dbSNP: rs12301299
rs12301299
WNK1
12 882544 intron variant T/C;G snv
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement 		0.700 1.000 1 2018 2018
dbSNP: rs12828016
rs12828016
WNK1
12 889199 missense variant G/T snv 0.37 0.41
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 1 2018 2018
dbSNP: rs12828016
rs12828016
WNK1
12 889199 missense variant G/T snv 0.37 0.41
CUI: C0205682
Disease: Waist-Hip Ratio
Waist-Hip Ratio 		0.700 1.000 1 2019 2019
dbSNP: rs34880640
rs34880640
WNK1
12 754011 missense variant C/T snv 3.3E-03 1.0E-03
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease 		0.010 1.000 1 2011 2011
dbSNP: rs55726687
rs55726687
WNK1
12 882140 intron variant G/A snv 0.17
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 1 2019 2019
dbSNP: rs72650721
rs72650721
WNK1
12 883487 synonymous variant G/A snv 4.4E-04 1.7E-03
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2012 2012
dbSNP: rs7305099
rs7305099
WNK1
12 866110 non coding transcript exon variant T/A;G snv
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease 		0.010 1.000 1 2019 2019
dbSNP: rs7955371
rs7955371
WNK1
12 885321 missense variant G/C snv 1.00 0.99
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.700 1.000 1 2012 2012
dbSNP: rs563030804
rs563030804
WNK1
1.000 0.040 12 868394 missense variant G/A snv 4.0E-06 7.0E-06
CUI: C0877015
Disease: Pelvic Organ Prolapse
Pelvic Organ Prolapse 		0.010 1.000 1 2015 2015
dbSNP: rs4619206
rs4619206
WNK1
1.000 0.080 12 893691 intron variant T/C snv 0.74
CUI: C0684249
Disease: Carcinoma of lung
Carcinoma of lung 		0.700 1.000 1 2017 2017
dbSNP: rs563691424
rs563691424
WNK1
1.000 0.080 12 753860 missense variant C/T snv 6.2E-05 2.1E-05
CUI: C0153381
Disease: Malignant neoplasm of mouth
Malignant neoplasm of mouth 		0.010 1.000 1 2015 2015
dbSNP: rs563691424
rs563691424
WNK1
1.000 0.080 12 753860 missense variant C/T snv 6.2E-05 2.1E-05
CUI: C0220641
Disease: Lip and Oral Cavity Carcinoma
Lip and Oral Cavity Carcinoma 		0.010 1.000 1 2015 2015
dbSNP: rs7953330
rs7953330
WNK1
0.925 0.080 12 889653 intron variant G/C snv 0.28
CUI: C0149782
Disease: Squamous cell carcinoma of lung
Squamous cell carcinoma of lung 		0.700 1.000 1 2017 2017
dbSNP: rs7953330
rs7953330
WNK1
0.925 0.080 12 889653 intron variant G/C snv 0.28
CUI: C0684249
Disease: Carcinoma of lung
Carcinoma of lung 		0.700 1.000 1 2017 2017
dbSNP: rs111033590
rs111033590
WNK1
0.925 0.080 12 868772 stop gained C/T snv 2.0E-05
CUI: C0020072
Disease: Hereditary Sensory Autonomic Neuropathy, Type 2
Hereditary Sensory Autonomic Neuropathy, Type 2 		0.700 0
dbSNP: rs111033590
rs111033590
WNK1
0.925 0.080 12 868772 stop gained C/T snv 2.0E-05
CUI: C2752089
Disease: Neuropathy, Hereditary Sensory And Autonomic, Type IIA
Neuropathy, Hereditary Sensory And Autonomic, Type IIA 		0.700 0
dbSNP: rs111033592
rs111033592
WNK1
1.000 0.080 12 868046 stop gained C/T snv
CUI: C2752089
Disease: Neuropathy, Hereditary Sensory And Autonomic, Type IIA
Neuropathy, Hereditary Sensory And Autonomic, Type IIA 		0.700 0
dbSNP: rs137852734
rs137852734
WNK1
1.000 0.080 12 868422 frameshift variant A/- delins
CUI: C0020072
Disease: Hereditary Sensory Autonomic Neuropathy, Type 2
Hereditary Sensory Autonomic Neuropathy, Type 2 		0.700 0