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: rs1064797103
rs1064797103
9 0.827 0.280 8 91078597 missense variant A/G snv 0.800 0
dbSNP: rs1064797102
rs1064797102
15 0.827 0.120 8 91071136 splice acceptor variant A/G snv 0.700 0
dbSNP: rs150848976
rs150848976
1 1.000 8 91080726 missense variant T/C snv 9.7E-05 1.5E-04 0.700 0
dbSNP: rs368313959
rs368313959
8 0.851 0.080 8 91078383 stop gained C/T snv 1.6E-04 1.0E-04 0.700 0
dbSNP: rs759317757
rs759317757
12 0.807 0.280 8 91078416 frameshift variant TTAAC/- delins 0.700 0