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: rs121434373
rs121434373
GCDH
1 1.000 0.120 19 12896249 missense variant G/A;C snv 1.6E-05; 1.8E-04 0.820 1.000 24 1995 2020
dbSNP: rs142967670
rs142967670
GCDH
1 1.000 0.120 19 12891965 missense variant C/A;T snv 4.0E-06; 4.8E-05 0.800 1.000 21 1995 2017
dbSNP: rs121434371
rs121434371
GCDH
1 1.000 0.120 19 12896934 missense variant G/A;T snv 6.0E-05; 4.0E-06 0.800 1.000 17 1995 2014
dbSNP: rs777201305
rs777201305
GCDH
1 1.000 0.120 19 12893630 missense variant G/A snv 3.6E-05 1.4E-05 0.800 1.000 16 1995 2018
dbSNP: rs781477694
rs781477694
GCDH
1 1.000 0.120 19 12897409 missense variant C/T snv 4.0E-06; 3.2E-05 3.5E-05 0.800 1.000 16 1995 2019
dbSNP: rs786204626
rs786204626
GCDH ; SYCE2
1 1.000 0.120 19 12897825 missense variant G/A snv 4.0E-06 0.800 1.000 16 1995 2017
dbSNP: rs150938052
rs150938052
GCDH ; SYCE2
1 1.000 0.120 19 12897767 missense variant C/T snv 1.6E-05 7.0E-05 0.800 1.000 15 1995 2014
dbSNP: rs121434367
rs121434367
GCDH ; SYCE2
1 1.000 0.120 19 12899486 missense variant C/T snv 1.2E-04 2.7E-04 0.810 1.000 14 1991 2017
dbSNP: rs121434369
rs121434369
GCDH ; SYCE2
1 1.000 0.120 19 12897824 missense variant C/T snv 3.2E-04 1.9E-04 0.810 1.000 14 1995 2017
dbSNP: rs121434372
rs121434372
GCDH ; SYCE2
1 1.000 0.120 19 12897818 missense variant G/A snv 1.1E-04 1.4E-04 0.820 1.000 14 1995 2016
dbSNP: rs139851890
rs139851890
GCDH
1 1.000 0.120 19 12893564 missense variant C/G;T snv 1.6E-05 1.4E-05 0.800 1.000 11 1995 2014
dbSNP: rs372983141
rs372983141
GCDH ; SYCE2
1 1.000 0.120 19 12897788 missense variant G/C snv 1.2E-05 5.6E-05 0.800 1.000 10 1995 2014
dbSNP: rs766518430
rs766518430
GCDH
1 1.000 0.120 19 12896338 missense variant C/T snv 2.0E-05 2.8E-05 0.700 1.000 10 1998 2015
dbSNP: rs778153326
rs778153326
GCDH ; SYCE2
1 1.000 0.120 19 12897789 missense variant G/C;T snv 4.0E-06 0.800 1.000 10 1995 2014
dbSNP: rs1555749239
rs1555749239
GCDH
1 1.000 0.120 19 12891895 missense variant G/T snv 0.810 1.000 9 1995 2014
dbSNP: rs121434370
rs121434370
GCDH
1 1.000 0.120 19 12897713 missense variant G/A snv 2.8E-05 4.2E-05 0.800 1.000 8 1995 2014
dbSNP: rs199999619
rs199999619
GCDH ; SYCE2
1 1.000 0.120 19 12899466 splice acceptor variant A/C;G snv 8.8E-05 2.8E-05 0.700 1.000 8 2000 2019
dbSNP: rs886043840
rs886043840
GCDH
1 1.000 0.120 19 12893504 missense variant C/T snv 1.2E-05 7.0E-06 0.700 1.000 8 2000 2017
dbSNP: rs1205368991
rs1205368991
GCDH
1 1.000 0.120 19 12896980 missense variant G/C snv 1.4E-05 0.700 1.000 7 1995 2014
dbSNP: rs121434366
rs121434366
GCDH
1 1.000 0.120 19 12896940 missense variant T/C snv 0.800 1.000 7 1995 2014
dbSNP: rs1282266790
rs1282266790
GCDH ; SYCE2
1 1.000 0.120 19 12897794 missense variant A/G snv 4.0E-06 0.700 1.000 7 1995 2014
dbSNP: rs151201155
rs151201155
GCDH ; SYCE2
1 1.000 0.120 19 12899485 missense variant G/A snv 2.0E-04 6.0E-04 0.700 1.000 7 1995 2014
dbSNP: rs1555751379
rs1555751379
GCDH ; SYCE2
1 1.000 0.120 19 12897840 missense variant T/C snv 0.700 1.000 7 1995 2014
dbSNP: rs566417795
rs566417795
GCDH
1 1.000 0.120 19 12892125 missense variant G/A;T snv 1.2E-04; 4.0E-06 0.800 1.000 7 1995 2014
dbSNP: rs745357523
rs745357523
GCDH
1 1.000 0.120 19 12896365 missense variant A/C;G snv 4.0E-06 0.700 1.000 7 1995 2014