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: rs1555493029
rs1555493029
10 0.851 0.240 16 23406263 splice acceptor variant C/A snv 0.700 0
dbSNP: rs1555496968
rs1555496968
1 1.000 0.080 16 23445968 splice region variant T/C snv 0.700 0
dbSNP: rs1555497568
rs1555497568
1 1.000 0.080 16 23452822 splice region variant T/G snv 0.700 0
dbSNP: rs1555497604
rs1555497604
10 0.851 0.240 16 23452993 start lost A/G snv 0.700 0