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: rs1555896285
rs1555896285
2 1.000 0.120 22 37725698 frameshift variant AG/- delins 0.700 0
dbSNP: rs1569034190
rs1569034190
2 1.000 0.120 22 37710443 stop gained C/G snv 0.700 0
dbSNP: rs1569040134
rs1569040134
2 1.000 0.120 22 37723382 missense variant C/T snv 0.700 0
dbSNP: rs1569042693
rs1569042693
2 1.000 0.120 22 37726080 stop gained C/A snv 0.700 0
dbSNP: rs1569042782
rs1569042782
2 1.000 0.120 22 37726189 frameshift variant CTGATCCCCCAAG/- delins 0.700 0
dbSNP: rs1569046250
rs1569046250
2 1.000 0.120 22 37734627 stop gained G/T snv 0.700 0