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: rs1564421528
rs1564421528
WAC
16 0.882 0.080 10 28614666 stop gained C/T snv 0.700 0
dbSNP: rs1085307139
rs1085307139
5 0.925 0.040 8 143817380 frameshift variant -/C delins 0.700 0
dbSNP: rs1114167294
rs1114167294
4 0.925 6 41587455 frameshift variant T/- del 0.700 0
dbSNP: rs1218912272
rs1218912272
8 0.925 0.160 1 152314342 stop gained T/A snv 4.0E-06 0.700 0
dbSNP: rs1554641549
rs1554641549
3 0.925 0.080 8 143816613 frameshift variant TGGCCTTATGA/- delins 0.700 0
dbSNP: rs1554643142
rs1554643142
4 0.925 0.120 8 143818042 frameshift variant CCTGCCCTATGTTGCTGGG/- delins 0.700 0
dbSNP: rs1559662068
rs1559662068
10 0.925 3 9741340 frameshift variant AG/T delins 0.700 0
dbSNP: rs527624522
rs527624522
5 0.925 0.080 11 44107723 missense variant C/T snv 6.4E-05 2.1E-05 0.700 0
dbSNP: rs1554817910
rs1554817910
4 1.000 10 79216266 missense variant A/G snv 0.700 1.000 1 2019 2019
dbSNP: rs724159948
rs724159948
7 1.000 21 37490273 stop gained C/T snv 0.700 0
dbSNP: rs724159950
rs724159950
6 1.000 0.200 21 37486571 frameshift variant TGAG/GAA delins 0.700 0
dbSNP: rs724159953
rs724159953
7 1.000 21 37505352 stop gained C/T snv 0.700 0