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: rs61755802
rs61755802
PRPH2
1 1.000 0.040 6 42704556 missense variant A/G snv 4.0E-06 0.800 1.000 4 1993 2016
dbSNP: rs61755789
rs61755789
PRPH2
1 0.925 0.080 6 42721835 missense variant C/T snv 0.800 0
dbSNP: rs61755809
rs61755809
PRPH2
1 0.925 0.080 6 42704535 missense variant G/A;T snv 4.0E-06 0.700 1.000 4 1993 2016
dbSNP: rs61755810
rs61755810
PRPH2
1 1.000 0.040 6 42704534 missense variant C/T snv 8.0E-06 7.0E-06 0.700 1.000 4 1993 2016
dbSNP: rs527236098
rs527236098
PRPH2
1 0.925 0.080 6 42721836 missense variant C/T snv 0.700 0
dbSNP: rs61755774
rs61755774
PRPH2
1 1.000 0.040 6 42722133 missense variant C/T snv 4.0E-06 0.700 0
dbSNP: rs61755787
rs61755787
PRPH2
1 0.882 0.120 6 42721866 missense variant C/T snv 0.700 0
dbSNP: rs61755792
rs61755792
PRPH2
1 0.763 0.160 6 42721821 missense variant G/A;C snv 0.700 0
dbSNP: rs61755798
rs61755798
PRPH2
2 0.827 0.080 6 42704564 missense variant G/A;C snv 0.700 0