Source: CURATED

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: rs11466112
rs11466112
1.000 0.080 1 115286135 missense variant G/A snv 1.6E-05 7.0E-06
Hereditary Sensory Autonomic Neuropathy, Type 5
0.710 1.000 0 2019 2019
dbSNP: rs11102916
rs11102916
1 115294125 intron variant C/A snv 3.7E-02
CUI: C0428883
Disease: Diastolic blood pressure
Diastolic blood pressure
0.700 1.000 1 2017 2017
dbSNP: rs11102916
rs11102916
1 115294125 intron variant C/A snv 3.7E-02
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure
0.700 1.000 1 2017 2017
dbSNP: rs11466111
rs11466111
1 115286557 missense variant C/T snv 1.0E-02 1.2E-02
CUI: C0428883
Disease: Diastolic blood pressure
Diastolic blood pressure
0.700 1.000 1 2017 2017
dbSNP: rs145339349
rs145339349
1 115288581 intron variant G/A snv 1.2E-02
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure
0.700 1.000 1 2019 2019
dbSNP: rs35225488
rs35225488
1 115309411 intron variant A/G snv 9.7E-02
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement
0.700 1.000 1 2019 2019
dbSNP: rs7523654
rs7523654
1.000 0.040 1 115318644 intron variant T/C snv 0.55
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
0.700 1.000 1 2019 2019