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: rs10037055
rs10037055
5 177264278 intron variant T/G snv 0.71
CUI: C2239219
Disease: von Willebrand's factor (lab test)
von Willebrand's factor (lab test)
0.700 1.000 1 2013 2013
dbSNP: rs10039241
rs10039241
5 177151071 intron variant G/A snv 0.26
CUI: C2239219
Disease: von Willebrand's factor (lab test)
von Willebrand's factor (lab test)
0.700 1.000 1 2013 2013
dbSNP: rs10056655
rs10056655
5 177249350 intron variant T/C snv 0.77
CUI: C2239219
Disease: von Willebrand's factor (lab test)
von Willebrand's factor (lab test)
0.700 1.000 1 2013 2013
dbSNP: rs10072499
rs10072499
5 177228236 intron variant T/G snv 0.23
CUI: C2239219
Disease: von Willebrand's factor (lab test)
von Willebrand's factor (lab test)
0.700 1.000 1 2013 2013
dbSNP: rs10077929
rs10077929
5 177270843 intron variant C/T snv 0.63
CUI: C2239219
Disease: von Willebrand's factor (lab test)
von Willebrand's factor (lab test)
0.700 1.000 1 2013 2013
dbSNP: rs10476217
rs10476217
5 177132734 upstream gene variant G/C snv 0.33
CUI: C0596887
Disease: mathematical ability
mathematical ability
0.700 1.000 1 2018 2018
dbSNP: rs1052432
rs1052432
5 177137188 3 prime UTR variant G/A snv 0.17
CUI: C2239219
Disease: von Willebrand's factor (lab test)
von Willebrand's factor (lab test)
0.700 1.000 1 2013 2013
dbSNP: rs114167666
rs114167666
5 177226053 intron variant G/A snv 1.5E-02
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 1 2019 2019
dbSNP: rs11949435
rs11949435
5 177287931 intron variant C/G snv 0.63
CUI: C2239219
Disease: von Willebrand's factor (lab test)
von Willebrand's factor (lab test)
0.700 1.000 1 2013 2013
dbSNP: rs11950938
rs11950938
5 177149292 intron variant C/A;G;T snv
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 1 2014 2014
dbSNP: rs11955537
rs11955537
5 177147087 intron variant A/C;G snv
CUI: C2239219
Disease: von Willebrand's factor (lab test)
von Willebrand's factor (lab test)
0.700 1.000 1 2013 2013
dbSNP: rs11957608
rs11957608
5 177228344 intron variant T/C snv 0.26
CUI: C2239219
Disease: von Willebrand's factor (lab test)
von Willebrand's factor (lab test)
0.700 1.000 1 2013 2013
dbSNP: rs12658510
rs12658510
5 177178272 intron variant G/A snv 0.14
CUI: C2239219
Disease: von Willebrand's factor (lab test)
von Willebrand's factor (lab test)
0.700 1.000 1 2013 2013
dbSNP: rs12660023
rs12660023
5 177273884 intron variant G/A snv 0.63
CUI: C2239219
Disease: von Willebrand's factor (lab test)
von Willebrand's factor (lab test)
0.700 1.000 1 2013 2013
dbSNP: rs1363405
rs1363405
5 177209881 synonymous variant C/T snv 0.29 0.36
CUI: C2239219
Disease: von Willebrand's factor (lab test)
von Willebrand's factor (lab test)
0.700 1.000 1 2013 2013
dbSNP: rs146677409
rs146677409
5 177165723 intron variant C/G snv 7.3E-03
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 1 2019 2019
dbSNP: rs1486617808
rs1486617808
5 177209916 missense variant C/T snv 1.4E-05
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
0.010 1.000 1 2018 2018
dbSNP: rs1486617808
rs1486617808
5 177209916 missense variant C/T snv 1.4E-05
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm
0.010 1.000 1 2018 2018
dbSNP: rs1546363
rs1546363
5 177174030 intron variant C/T snv 0.36
CUI: C2239219
Disease: von Willebrand's factor (lab test)
von Willebrand's factor (lab test)
0.700 1.000 1 2013 2013
dbSNP: rs2336237
rs2336237
5 177238878 intron variant G/A snv 0.64
CUI: C2239219
Disease: von Willebrand's factor (lab test)
von Willebrand's factor (lab test)
0.700 1.000 1 2013 2013
dbSNP: rs2431501
rs2431501
5 177179051 intron variant T/A;G snv
CUI: C2239219
Disease: von Willebrand's factor (lab test)
von Willebrand's factor (lab test)
0.700 1.000 1 2013 2013
dbSNP: rs2878686
rs2878686
5 177206748 intron variant C/T snv 0.26
CUI: C2239219
Disease: von Willebrand's factor (lab test)
von Willebrand's factor (lab test)
0.700 1.000 1 2013 2013
dbSNP: rs28932178
rs28932178
5 177210575 missense variant T/C snv 0.20 0.16
High density lipoprotein measurement
0.700 1.000 1 2017 2017
dbSNP: rs3088050
rs3088050
5 177299634 3 prime UTR variant G/A snv 0.18
CUI: C0205682
Disease: Waist-Hip Ratio
Waist-Hip Ratio
0.700 1.000 1 2019 2019
dbSNP: rs3088050
rs3088050
5 177299634 3 prime UTR variant G/A snv 0.18
CUI: C4049938
Disease: Physical Activity Measurement
Physical Activity Measurement
0.700 1.000 1 2017 2017