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: rs11602339
rs11602339
FNBP4
11 47739919 intron variant C/T snv 0.27
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 1 2017 2017
dbSNP: rs150341456
rs150341456
FNBP4
11 47762062 intron variant T/A;C snv
CUI: C1861172
Disease: Venous Thromboembolism
Venous Thromboembolism 		0.700 1.000 1 2019 2019
dbSNP: rs150341456
rs150341456
FNBP4
11 47762062 intron variant T/A;C snv
CUI: C0042487
Disease: Venous Thrombosis
Venous Thrombosis 		0.700 1.000 1 2012 2012
dbSNP: rs17788930
rs17788930
FNBP4
11 47731223 intron variant A/G snv 0.27
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.700 1.000 1 2019 2019
dbSNP: rs34923397
rs34923397
FNBP4
11 47748012 intron variant G/A snv 0.26
CUI: C0021704
Disease: Intelligence
Intelligence 		0.700 1.000 1 2018 2018
dbSNP: rs78261087
rs78261087
FNBP4
11 47743354 intron variant G/A;T snv 2.0E-02
CUI: C0042487
Disease: Venous Thrombosis
Venous Thrombosis 		0.700 1.000 1 2012 2012