Gene: WNT16 ×
Source: ALL
Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs3801387
rs3801387
WNT16
2 7 121334711 intron variant A/C;G snv 0.700 1.000 3 2012 2014
dbSNP: rs2908004
rs2908004
WNT16
4 1.000 0.040 7 121329715 missense variant G/A;T snv 0.44; 4.0E-06 0.700 1.000 2 2012 2012
dbSNP: rs2536189
rs2536189
WNT16
1 7 121333567 intron variant C/G snv 0.55 0.700 1.000 1 2012 2012
dbSNP: rs2707466
rs2707466
WNT16
2 1.000 0.040 7 121339035 missense variant C/G;T snv 0.44 0.700 1.000 1 2012 2012
dbSNP: rs3757552
rs3757552
WNT16
1 7 121323911 upstream gene variant A/G;T snv 0.700 1.000 1 2012 2012
dbSNP: rs3779381
rs3779381
WNT16
3 0.925 0.160 7 121326736 intron variant A/G snv 0.29 0.700 1.000 1 2012 2012
dbSNP: rs3801385
rs3801385
WNT16
1 7 121337489 intron variant T/C snv 8.2E-02 0.700 1.000 1 2012 2012