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: rs59897026
rs59897026
KRT13
2 0.925 0.200 17 41505219 missense variant A/G snv 0.800 0
dbSNP: rs60440396
rs60440396
KRT13
1 1.000 17 41505195 missense variant A/G snv 0.800 0
dbSNP: rs60364670
rs60364670
KRT13
1 1.000 17 41505228 start lost A/G snv 0.700 1.000 4 1995 2003
dbSNP: rs59970018
rs59970018
KRT13
1 1.000 17 41505216 missense variant T/C snv 0.700 0
dbSNP: rs60906702
rs60906702
KRT13
1 1.000 17 41505207 missense variant A/G snv 0.700 0