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: rs137852959
rs137852959
PANK2 ; MIR103B2
9 0.790 0.160 20 3918695 missense variant G/A snv 8.7E-05 2.3E-04 0.700 0
dbSNP: rs137852964
rs137852964
PANK2
2 0.925 0.080 20 3910646 missense variant T/C snv 0.700 0
dbSNP: rs137852965
rs137852965
PANK2
2 0.925 0.080 20 3907997 missense variant A/G snv 1.6E-05 7.0E-06 0.700 0
dbSNP: rs137852966
rs137852966
PANK2
2 0.925 0.080 20 3908129 missense variant C/T snv 8.0E-06 0.700 0
dbSNP: rs137852967
rs137852967
PANK2 ; MIR103B2
3 0.882 0.080 20 3918717 missense variant C/T snv 1.2E-05 2.1E-05 0.700 0