Gene: PRPH2 ×
Source: UNIPROT ×
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: rs61755806
rs61755806
PRPH2
1 0.882 0.080 6 42704546 missense variant G/A snv 4.0E-06 7.0E-06 0.800 1.000 11 1991 2016
dbSNP: rs61755816
rs61755816
PRPH2
1 0.925 0.080 6 42704461 missense variant G/C;T snv 0.800 1.000 11 1991 2016
dbSNP: rs61755794
rs61755794
PRPH2
1 1.000 0.080 6 42721817 missense variant T/A snv 0.800 0
dbSNP: rs121918563
rs121918563
PRPH2
1 0.827 0.120 6 42721781 missense variant A/G snv 8.0E-06 1.4E-05 0.700 1.000 11 1991 2016
dbSNP: rs139185976
rs139185976
PRPH2
1 0.882 0.080 6 42704570 missense variant C/T snv 4.8E-05 9.8E-05 0.700 1.000 11 1991 2016
dbSNP: rs61755800
rs61755800
PRPH2
1 0.882 0.080 6 42704559 missense variant T/C;G snv 8.0E-06 0.700 1.000 11 1991 2016
dbSNP: rs61755804
rs61755804
PRPH2
1 0.925 0.080 6 42704552 missense variant C/G;T snv 0.700 1.000 11 1991 2016
dbSNP: rs61755805
rs61755805
PRPH2
1 0.882 0.080 6 42704547 missense variant G/A snv 0.700 1.000 11 1991 2016
dbSNP: rs61754402
rs61754402
PRPH2
1 1.000 0.080 6 42722298 missense variant G/A;T snv 4.3E-04 0.700 0
dbSNP: rs61755770
rs61755770
PRPH2
2 0.925 0.080 6 42722202 missense variant G/A snv 1.1E-03 4.1E-03 0.700 0
dbSNP: rs61755781
rs61755781
PRPH2
2 0.851 0.080 6 42721913 missense variant T/C snv 0.700 0
dbSNP: rs61755783
rs61755783
PRPH2
1 0.763 0.080 6 42721911 missense variant G/A snv 1.4E-05 0.700 0
dbSNP: rs61755785
rs61755785
PRPH2
1 1.000 0.080 6 42721877 missense variant T/C snv 0.700 0
dbSNP: rs61755788
rs61755788
PRPH2
1 1.000 0.080 6 42721841 missense variant C/T snv 0.700 0
dbSNP: rs61755797
rs61755797
PRPH2
1 0.882 0.080 6 42704565 missense variant G/A;C snv 4.0E-06 0.700 0
dbSNP: rs61755798
rs61755798
PRPH2
2 0.827 0.080 6 42704564 missense variant G/A;C snv 0.700 0
dbSNP: rs61755799
rs61755799
PRPH2
1 0.882 0.160 6 42704560 missense variant G/T snv 0.700 0
dbSNP: rs62645935
rs62645935
PRPH2
1 0.925 0.080 6 42704396 missense variant C/T snv 0.700 0