Source: GWASCAT

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: rs1440371
rs1440371
LINC01169
15 66648746 intron variant G/A snv 0.27
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure 		0.700 1.000 2 2019 2019
dbSNP: rs11377084
rs11377084
LINC01169
15 66651883 intron variant -/A ins 0.67
CUI: C0518015
Disease: Hemoglobin measurement
Hemoglobin measurement 		0.700 1.000 1 2016 2016
dbSNP: rs1440371
rs1440371
LINC01169
15 66648746 intron variant G/A snv 0.27
CUI: C0007222
Disease: Cardiovascular Diseases
Cardiovascular Diseases 		0.700 1.000 1 2019 2019
dbSNP: rs16950081
rs16950081
LINC01169
15 66630879 intron variant G/A snv 5.3E-02
CUI: C0201534
Disease: Antiphospholipid antibodies measurement
Antiphospholipid antibodies measurement 		0.700 1.000 1 2016 2016
dbSNP: rs1866750
rs1866750
LINC01169
15 66615205 intron variant T/C snv 0.26
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs2245586
rs2245586
LINC01169
15 66586562 intron variant A/G snv 0.73
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.700 1.000 1 2018 2018
dbSNP: rs8023793
rs8023793
LINC01169
1.000 0.080 15 66649755 intron variant C/A snv 0.46
CUI: C0600139
Disease: Prostate carcinoma
Prostate carcinoma 		0.700 1.000 1 2019 2019
dbSNP: rs8030097
rs8030097
LINC01169
15 66651066 intron variant C/A;G;T snv
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement 		0.700 1.000 1 2019 2019
dbSNP: rs893907
rs893907
LINC01169
15 66630557 intron variant C/G snv 0.50
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: rs893907
rs893907
LINC01169
15 66630557 intron variant C/G snv 0.50
CUI: C0427460
Disease: Red cell distribution width determination
Red cell distribution width determination 		0.700 1.000 1 2019 2019