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: rs113798404
rs113798404
CDKN2A
2 0.925 0.080 9 21970995 missense variant C/G;T snv 0.700 0
dbSNP: rs199907548
rs199907548
CDKN2A
5 0.882 0.160 9 21974682 missense variant A/C;G snv 6.3E-04 0.700 0
dbSNP: rs760065045
rs760065045
CDKN2A
1 1.000 0.080 9 21974770 missense variant C/A;G snv 4.3E-06 0.700 0