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: rs63750410
rs63750410
ABCC6
9 0.882 0.240 16 16155007 missense variant C/G;T snv 6.0E-06; 1.2E-05 0.700 0
dbSNP: rs63750428
rs63750428
ABCC6
6 0.925 0.200 16 16154767 missense variant G/A;T snv 4.9E-05 0.700 0
dbSNP: rs63750459
rs63750459
ABCC6
13 0.851 0.320 16 16163110 missense variant G/A snv 6.8E-05 6.3E-05 0.700 0
dbSNP: rs63750622
rs63750622
ABCC6
9 0.925 0.200 16 16154898 missense variant C/A;G;T snv 4.1E-06; 4.1E-06; 1.6E-05 0.700 0
dbSNP: rs63750759
rs63750759
ABCC6
11 0.851 0.280 16 16154974 missense variant G/A;T snv 1.9E-04; 5.4E-06 0.700 0
dbSNP: rs63751001
rs63751001
ABCC6
13 0.790 0.240 16 16159555 missense variant C/T snv 2.8E-05 0.700 0
dbSNP: rs63751111
rs63751111
ABCC6
7 1.000 0.160 16 16154873 missense variant C/G;T snv 8.1E-06 0.700 0
dbSNP: rs63751241
rs63751241
ABCC6
12 0.882 0.280 16 16154638 missense variant C/T snv 4.0E-05 1.4E-05 0.700 0
dbSNP: rs66864704
rs66864704
ABCC6
10 0.882 0.280 16 16188907 missense variant A/G snv 1.2E-04 3.6E-04 0.700 0
dbSNP: rs72653761
rs72653761
ABCC6
7 0.925 0.200 16 16202033 missense variant G/A snv 5.2E-05 6.3E-05 0.700 0
dbSNP: rs72653762
rs72653762
ABCC6
13 0.851 0.240 16 16202006 missense variant T/C snv 5.6E-03 4.7E-03 0.700 0
dbSNP: rs72653769
rs72653769
ABCC6
6 1.000 0.160 16 16190315 missense variant A/T snv 8.0E-06 0.700 0
dbSNP: rs72653772
rs72653772
ABCC6
16 0.807 0.320 16 16190246 missense variant C/T snv 8.4E-05 1.1E-04 0.700 0
dbSNP: rs72653777
rs72653777
ABCC6
6 1.000 0.160 16 16187193 missense variant G/A snv 2.8E-05 4.2E-05 0.700 0
dbSNP: rs72653783
rs72653783
ABCC6
7 1.000 0.160 16 16182566 missense variant T/G snv 4.0E-06 0.700 0
dbSNP: rs72653784
rs72653784
ABCC6
5 1.000 0.160 16 16182562 missense variant C/A;T snv 2.0E-05; 4.0E-06 0.700 0
dbSNP: rs72653787
rs72653787
ABCC6
9 0.925 0.200 16 16178950 missense variant C/T snv 3.6E-05 3.5E-05 0.700 0
dbSNP: rs72653788
rs72653788
ABCC6
8 1.000 0.160 16 16178935 missense variant G/A snv 3.2E-05 5.6E-05 0.700 0
dbSNP: rs72653794
rs72653794
ABCC6
9 0.882 0.280 16 16177622 missense variant C/T snv 2.4E-05 2.8E-05 0.700 0
dbSNP: rs749125777
rs749125777
ABCC6
6 1.000 0.160 16 16173287 missense variant G/A;C snv 4.0E-06; 8.0E-06 0.700 0
dbSNP: rs761433545
rs761433545
ABCC6
8 0.925 0.200 16 16187192 missense variant C/A;G;T snv 2.0E-05 0.700 0
dbSNP: rs776513864
rs776513864
ABCC6
6 0.925 0.200 16 16178920 missense variant G/A;C snv 1.2E-05; 4.0E-06 0.700 0
dbSNP: rs78678589
rs78678589
ABCC6
8 0.925 0.160 16 16203457 missense variant G/C;T snv 1.6E-05 0.700 0
dbSNP: rs965791272
rs965791272
ABCC6
6 1.000 0.160 16 16155041 non coding transcript exon variant G/A;C;T snv 0.700 0
dbSNP: rs5443
rs5443
GNB3 ; CDCA3
106 0.532 0.760 12 6845711 synonymous variant C/T snv 0.36 0.44 0.010 1.000 1 2006 2006