Gene: BCHE ×
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: rs1803274
rs1803274
BCHE
13 0.763 0.360 3 165773492 missense variant C/T snv 0.18 0.18 0.800 1.000 2 2011 2011
dbSNP: rs12053876
rs12053876
BCHE
1 3 165832595 intron variant G/A snv 0.77 0.700 1.000 1 2011 2011
dbSNP: rs12107166
rs12107166
BCHE
1 3 165779505 intron variant T/G snv 0.13 0.700 1.000 1 2011 2011
dbSNP: rs12186091
rs12186091
BCHE
1 3 165799802 intron variant C/A snv 9.6E-02 0.700 1.000 1 2011 2011
dbSNP: rs12487357
rs12487357
BCHE
1 3 165804028 intron variant G/A;C snv 0.700 1.000 1 2011 2011
dbSNP: rs1355535
rs1355535
BCHE
1 3 165787971 intron variant T/G snv 0.58 0.700 1.000 1 2011 2011
dbSNP: rs1355538
rs1355538
BCHE
1 3 165787389 intron variant A/G snv 0.43 0.700 1.000 1 2011 2011
dbSNP: rs16849623
rs16849623
BCHE
1 3 165782372 intron variant G/T snv 6.5E-02 0.700 1.000 1 2011 2011
dbSNP: rs16849671
rs16849671
BCHE
1 3 165809591 intron variant C/A snv 9.5E-02 0.700 1.000 1 2011 2011
dbSNP: rs2048493
rs2048493
BCHE
1 3 165826514 intron variant G/A;C;T snv 0.700 1.000 1 2011 2011
dbSNP: rs2089885
rs2089885
BCHE
1 3 165791453 intron variant G/A snv 0.65 0.700 1.000 1 2011 2011
dbSNP: rs2668196
rs2668196
BCHE
3 3 165784921 intron variant A/T snv 0.75 0.700 1.000 1 2011 2011
dbSNP: rs2668202
rs2668202
BCHE
1 3 165772680 intron variant A/G snv 0.51 0.700 1.000 1 2011 2011
dbSNP: rs2668203
rs2668203
BCHE
1 3 165774008 intron variant A/G snv 0.64 0.700 1.000 1 2011 2011
dbSNP: rs2668206
rs2668206
BCHE
1 3 165775666 intron variant A/C snv 0.51 0.700 1.000 1 2011 2011
dbSNP: rs2668207
rs2668207
BCHE
1 3 165775936 intron variant C/T snv 0.51 0.700 1.000 1 2011 2011
dbSNP: rs2668208
rs2668208
BCHE
1 3 165776031 intron variant A/G;T snv 0.700 1.000 1 2011 2011
dbSNP: rs2668209
rs2668209
BCHE
1 3 165776779 intron variant G/A;T snv 0.700 1.000 1 2011 2011
dbSNP: rs2686405
rs2686405
BCHE
1 3 165773977 intron variant G/C;T snv 0.700 1.000 1 2011 2011
dbSNP: rs2686409
rs2686409
BCHE
1 3 165777612 intron variant G/A snv 0.64 0.700 1.000 1 2011 2011
dbSNP: rs2686410
rs2686410
BCHE
1 3 165777632 intron variant G/C snv 0.51 0.700 1.000 1 2011 2011
dbSNP: rs3806650
rs3806650
BCHE
1 3 165838023 intron variant G/A snv 0.66 0.700 1.000 1 2011 2011
dbSNP: rs3863086
rs3863086
BCHE
1 3 165782897 intron variant C/A;T snv 5.8E-02 0.700 1.000 1 2011 2011
dbSNP: rs4465985
rs4465985
BCHE
1 3 165822154 intron variant A/T snv 7.2E-02 0.700 1.000 1 2011 2011
dbSNP: rs4563443
rs4563443
BCHE
1 3 165835049 intron variant C/A snv 8.3E-02 0.700 1.000 1 2011 2011