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: rs1566402656
rs1566402656
CRYAB
1 1.000 11 111908842 frameshift variant T/- delins 0.700 0
dbSNP: rs387907336
rs387907336
CRYAB
1 1.000 11 111908874 missense variant C/T snv 0.700 0
dbSNP: rs387907337
rs387907337
CRYAB ; HSPB2 ; HSPB2-C11orf52
1 1.000 11 111911667 missense variant G/A snv 0.700 0
dbSNP: rs387907338
rs387907338
CRYAB ; HSPB2 ; HSPB2-C11orf52
5 0.827 0.200 11 111911559 missense variant G/A;T snv 0.700 0