WNT2B, Wnt family member 2B, 7482

N. diseases: 65; N. variants: 12
Source: ALL
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs351364
rs351364
1 112502439 intron variant A/C;T snv 0.72
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure
0.700 1.000 1 2018 2018
dbSNP: rs1620668
rs1620668
1 112481358 intron variant A/G snv 0.17
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure
0.700 1.000 1 2016 2016
dbSNP: rs3790604
rs3790604
1 112504257 intron variant C/A snv 7.8E-02
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure
0.700 1.000 3 2018 2019
dbSNP: rs10776752
rs10776752
1 112501706 intron variant G/T snv 8.8E-02
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure
0.700 1.000 2 2018 2019