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: rs28931603
rs28931603
CPOX
2 0.925 0.160 3 98580709 missense variant G/A snv 4.0E-04 2.7E-04 0.810 1.000 10 1994 2006
dbSNP: rs121917868
rs121917868
CPOX
3 0.882 0.160 3 98581474 missense variant T/C snv 4.0E-05 8.4E-05 0.710 1.000 11 1994 2006
dbSNP: rs121917866
rs121917866
CPOX
2 0.925 0.160 3 98585622 missense variant G/A snv 4.0E-06 0.710 1.000 10 1994 2006
dbSNP: rs121917870
rs121917870
CPOX
2 0.925 0.160 3 98588783 missense variant G/A;C snv 0.700 1.000 10 1994 2006
dbSNP: rs121917872
rs121917872
CPOX
2 0.925 0.160 3 98591089 missense variant G/A snv 0.700 1.000 10 1994 2006
dbSNP: rs121917873
rs121917873
CPOX
2 0.925 0.160 3 98585631 missense variant G/A snv 7.0E-06 0.700 1.000 10 1994 2006
dbSNP: rs121917874
rs121917874
CPOX
2 0.925 0.160 3 98588831 missense variant C/G snv 0.700 1.000 10 1994 2006
dbSNP: rs201826432
rs201826432
CPOX
1 1.000 0.160 3 98593101 missense variant A/G snv 4.0E-06 2.1E-05 0.700 1.000 10 1994 2006
dbSNP: rs759347283
rs759347283
CPOX
1 1.000 0.160 3 98591147 missense variant C/T snv 8.0E-06 2.1E-05 0.700 1.000 10 1994 2006
dbSNP: rs1374394802
rs1374394802
CPOX
1 1.000 0.160 3 98591111 missense variant C/T snv 1.2E-05 2.8E-05 0.700 0
dbSNP: rs28933068
rs28933068
FGFR3
30 0.645 0.560 4 1805644 missense variant C/A;G;T snv 1.6E-05 0.010 1.000 1 2012 2012