Source: CURATED ×
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: rs1057516264
rs1057516264
13 0.776 0.280 11 6614968 frameshift variant C/-;CC delins 0.700 0
dbSNP: rs1057518813
rs1057518813
8 0.790 0.240 13 102873305 frameshift variant CT/- delins 0.700 0
dbSNP: rs1057519429
rs1057519429
14 0.807 0.240 19 13235666 missense variant C/G;T snv 0.700 0
dbSNP: rs1114167295
rs1114167295
6 0.827 0.160 X 54812169 frameshift variant C/- del 0.700 0
dbSNP: rs1114167296
rs1114167296
6 0.827 0.160 X 34656995 missense variant C/G snv 0.700 0
dbSNP: rs1208636573
rs1208636573
15 0.807 0.120 1 155612098 stop gained C/G;T snv 4.0E-06; 4.0E-06 0.700 0
dbSNP: rs139632595
rs139632595
19 0.807 0.160 4 121801465 missense variant T/C snv 6.0E-05 2.5E-04 0.700 0
dbSNP: rs1553281318
rs1553281318
7 0.882 0.120 1 226986536 frameshift variant -/A delins 0.700 0
dbSNP: rs1554107200
rs1554107200
4 0.851 0.120 5 140679127 missense variant C/A snv 0.700 0
dbSNP: rs1554699491
rs1554699491
23 0.763 0.280 9 85596450 splice acceptor variant C/A snv 0.700 0
dbSNP: rs1554768245
rs1554768245
16 0.807 0.160 6 152472395 frameshift variant C/- delins 0.700 0
dbSNP: rs1554901898
rs1554901898
12 0.776 0.280 11 6616858 frameshift variant A/- delins 0.700 0
dbSNP: rs1554902217
rs1554902217
7 0.851 0.160 11 6618821 frameshift variant A/- del 0.700 0
dbSNP: rs1555570110
rs1555570110
9 0.827 0.240 17 7586766 missense variant A/C snv 0.700 0
dbSNP: rs1555642784
rs1555642784
5 0.851 0.160 17 42688979 frameshift variant -/C delins 0.700 0
dbSNP: rs1555745467
rs1555745467
23 0.752 0.240 19 13262771 missense variant C/A snv 0.700 0
dbSNP: rs1563390893
rs1563390893
CA8
5 0.851 0.200 8 60281047 splice donor variant C/T snv 0.700 0
dbSNP: rs201128942
rs201128942
5 0.851 0.120 6 85547112 stop gained C/A;T snv 2.4E-05 4.2E-05 0.700 0
dbSNP: rs28934907
rs28934907
29 0.732 0.320 X 154032268 missense variant G/A;C snv 0.700 0
dbSNP: rs387906799
rs387906799
17 0.742 0.200 2 240788118 missense variant G/A snv 0.700 0
dbSNP: rs587777721
rs587777721
4 0.925 0.160 12 51806336 missense variant G/A snv 0.700 0
dbSNP: rs622288
rs622288
15 0.807 0.120 1 155612848 missense variant C/T snv 3.6E-05 4.2E-05 0.700 0
dbSNP: rs672601362
rs672601362
7 0.851 0.080 2 240789246 missense variant G/A snv 0.700 0
dbSNP: rs672601363
rs672601363
6 0.851 0.080 2 240788109 missense variant C/T snv 0.700 0
dbSNP: rs672601367
rs672601367
7 0.851 0.080 2 240785066 missense variant T/G snv 0.700 0