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: rs149830411
rs149830411
15 0.827 0.360 17 46171276 stop gained G/A snv 5.2E-05 5.6E-05 0.700 0
dbSNP: rs1553553086
rs1553553086
9 0.827 0.280 2 222623699 missense variant C/T snv 0.700 0
dbSNP: rs1553603732
rs1553603732
DES
10 1.000 0.160 2 219423784 frameshift variant CCCATCCAGACCTACTC/- delins 0.700 0
dbSNP: rs1554121443
rs1554121443
29 0.742 0.280 6 33438873 stop gained C/T snv 0.700 0
dbSNP: rs1554317002
rs1554317002
45 0.724 0.440 7 39950821 frameshift variant C/- delins 0.700 0
dbSNP: rs1554863016
rs1554863016
5 0.882 0.240 10 92648211 splice acceptor variant G/A snv 0.700 0
dbSNP: rs1555055028
rs1555055028
5 0.882 0.160 11 124923996 missense variant G/A snv 0.700 0
dbSNP: rs1555377415
rs1555377415
18 0.827 0.200 14 77027274 stop gained G/C snv 0.700 0
dbSNP: rs1555429629
rs1555429629
23 0.763 0.200 15 40729632 missense variant G/A snv 0.700 0
dbSNP: rs1555740650
rs1555740650
13 0.807 0.240 19 49596253 stop gained G/T snv 0.700 0
dbSNP: rs1555745467
rs1555745467
23 0.752 0.240 19 13262771 missense variant C/A snv 0.700 0
dbSNP: rs1555928716
rs1555928716
7 0.925 X 20167669 stop gained G/A snv 0.700 0
dbSNP: rs1555968941
rs1555968941
31 0.752 0.280 12 2653847 missense variant G/A;C snv 0.700 0
dbSNP: rs1557644984
rs1557644984
5 0.925 0.080 1 42927622 missense variant A/G snv 0.700 0
dbSNP: rs1559759089
rs1559759089
14 0.827 0.200 3 113795101 missense variant C/A snv 0.700 0
dbSNP: rs1560212751
rs1560212751
2 1.000 3 51208772 splice acceptor variant A/G snv 0.700 0
dbSNP: rs1560414254
rs1560414254
2 1.000 3 51312486 frameshift variant ACTT/- delins 0.700 0
dbSNP: rs1560755661
rs1560755661
44 0.701 0.480 4 106171094 splice donor variant CAGATCTGTCTTTGGAGGATCTGGACACTCAGCAGAGAAATAAGGTGCCGAACTTCTGCCTCCACTGCTGTCAGAAGATGGCTTTGGAGGTTGAGCATGCTGTCTGTAAGTAGCACTTTTAGGAGTCCAACAAAACAGGTTGATAGATTCTCTCACACAGCGTTCAATGTCAATTTC/- delins 0.700 0
dbSNP: rs1567010427
rs1567010427
11 0.882 14 102010824 missense variant G/A snv 0.700 0
dbSNP: rs1567498374
rs1567498374
5 0.882 0.160 16 75630493 frameshift variant G/-;GG delins 0.700 0
dbSNP: rs1567941252
rs1567941252
10 0.807 0.240 17 38739601 missense variant G/A snv 0.700 0
dbSNP: rs1568507354
rs1568507354
6 0.827 0.200 19 38502879 splice acceptor variant G/A snv 0.700 0
dbSNP: rs1569110700
rs1569110700
5 0.925 0.080 22 42179633 missense variant G/A snv 0.700 0
dbSNP: rs1569548274
rs1569548274
43 0.701 0.520 X 154030553 splice acceptor variant TCCAGTGAGCCTCCTCTGGGCATCTTCTCCTCTTTGCAGACGCTGCTGCTCAAGTCCTGGGGCTCAGGGGGGCTGGTGGGGTCCTCGGAGCTCTCGGGCTCAGGTGGAGGTGGGGGCAGGGGTGGGAGCAGTGGCACGGGGGCCTTTGGGGACTCTGAGTGGTGGTGATGGTGGTGGTGCTCCTTCTTGGGGGGTGAGGAGGCGCTGCTGCTGCGCCCCTTGGGGCTGCTCTCCTTGCTTTTCCGCCCAGGGCTCTTACAGGTCTTCAGTCCTTTCCCGCTCTTCTCACCGAGGGTGGACACCAGCAGGGGCTTCACCACTTCCTTGACCTCGATGCTGACCGTCTCCCGGGTCTTGCGCTTCTTGATGGGGAGTACGGTCTCCTGCACAGATCGGATAGAAGACTCCTTCACGGCTTTCTTTTTGGCCTCGGCGGCAGCGGCTGCCACCACACTCCCCGGCTTTCGGCCCCGTTTCTTGGGAATGGCCTGAGGGTCGGCCTCAGCTTTTCGCTTCCTGCCGGGGCGTTTGATCACCATGACCTGGGTGGATGTGGTGGCCCCACCCCCCTCAGC/- delins 0.700 0
dbSNP: rs180177035
rs180177035
35 0.752 0.280 7 140801502 missense variant T/C snv 0.700 0