Source: ALL
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: rs1057519561
rs1057519561
SNX14
4 0.882 0.200 6 85533701 frameshift variant -/AAAAAAAAAAA delins 7.0E-06 0.700 0
dbSNP: rs1562374476
rs1562374476
SNX14
2 1.000 6 85572333 stop gained A/T snv 0.700 0
dbSNP: rs201128942
rs201128942
SNX14
5 0.851 0.120 6 85547112 stop gained C/A;T snv 2.4E-05 4.2E-05 0.700 0
dbSNP: rs760752847
rs760752847
SNX14
1 1.000 6 85572305 stop gained G/A snv 2.4E-05 0.700 0
dbSNP: rs774694340
rs774694340
SNX14
4 0.882 0.200 6 85508043 frameshift variant A/- del 6.4E-05 1.4E-05 0.700 0
dbSNP: rs786205229
rs786205229
SNX14
1 1.000 6 85543737 stop gained G/A snv 7.0E-06 0.700 0
dbSNP: rs869320748
rs869320748
SNX14
1 1.000 6 85549868 frameshift variant -/T delins 0.700 0
dbSNP: rs876657385
rs876657385
SNX14
1 1.000 6 85513857 stop gained G/A;C snv 8.0E-06 0.700 0
dbSNP: rs876657386
rs876657386
SNX14
1 1.000 6 85530191 splice donor variant C/A snv 0.700 0
dbSNP: rs876657387
rs876657387
SNX14
1 1.000 6 85567567 stop gained A/T snv 0.700 0