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: rs58730926
rs58730926
KRT17
2 0.925 0.080 17 41624230 missense variant G/A snv 1.4E-05 0.810 1.000 4 1997 2015
dbSNP: rs28928896
rs28928896
KRT17
2 0.925 0.080 17 41624236 missense variant T/C;G snv 0.810 1.000 3 1997 2006
dbSNP: rs28928898
rs28928898
KRT17
3 0.882 0.080 17 41624247 missense variant A/G;T snv 0.710 1.000 3 1997 2006
dbSNP: rs28928897
rs28928897
KRT17
2 0.925 0.080 17 41624229 missense variant C/G;T snv 0.710 1.000 1 1997 1997