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: rs121908068
rs121908068
1 1.000 0.040 5 177292124 missense variant C/G;T snv 7.6E-05 0.800 1.000 4 2002 2004
dbSNP: rs121908069
rs121908069
1 1.000 0.040 5 177293916 missense variant G/C snv 0.800 1.000 4 2002 2004
dbSNP: rs797045057
rs797045057
1 1.000 0.040 5 177282522 stop gained C/T snv 0.700 1.000 2 2005 2016
dbSNP: rs1562305653
rs1562305653
1 1.000 0.040 5 177292061 missense variant T/G snv 0.700 1.000 1 2016 2016
dbSNP: rs587784077
rs587784077
1 1.000 0.040 5 177210230 stop gained C/G;T snv 0.700 1.000 1 2005 2005
dbSNP: rs587784137
rs587784137
1 1.000 0.040 5 177260120 stop gained C/T snv 0.700 1.000 1 2007 2007
dbSNP: rs794729232
rs794729232
1 1.000 0.040 5 177210141 frameshift variant A/- delins 0.700 1.000 1 2003 2003
dbSNP: rs797045058
rs797045058
1 1.000 0.040 5 177295334 stop gained C/T snv 0.700 1.000 1 2016 2016
dbSNP: rs879253860
rs879253860
1 1.000 0.040 5 177293901 frameshift variant -/C delins 0.700 1.000 1 2015 2015
dbSNP: rs1006906224
rs1006906224
1 1.000 0.040 5 177211437 stop gained C/G;T snv 0.700 0
dbSNP: rs1131692328
rs1131692328
1 1.000 0.040 5 177209948 stop gained C/A;G;T snv 0.700 0
dbSNP: rs121908067
rs121908067
1 1.000 0.040 5 177209709 stop gained C/G snv 0.700 0
dbSNP: rs121908070
rs121908070
1 1.000 0.040 5 177238273 stop gained C/T snv 0.700 0
dbSNP: rs121908071
rs121908071
1 1.000 0.040 5 177293973 missense variant G/A snv 0.700 0
dbSNP: rs1286331975
rs1286331975
1 1.000 0.040 5 177210272 stop gained G/A;T snv 4.0E-06 0.700 0
dbSNP: rs1554189482
rs1554189482
1 1.000 0.040 5 177210710 frameshift variant G/- delins 0.700 0
dbSNP: rs1554189941
rs1554189941
1 1.000 0.040 5 177211403 frameshift variant AA/- del 0.700 0
dbSNP: rs1554189972
rs1554189972
1 1.000 0.040 5 177211433 stop gained -/TTCAGACTGTGTTACTAGG delins 0.700 0
dbSNP: rs1554195815
rs1554195815
1 1.000 0.040 5 177238235 splice acceptor variant AGGTAA/G delins 0.700 0
dbSNP: rs1554200207
rs1554200207
1 1.000 0.040 5 177260091 missense variant C/G snv 0.700 0
dbSNP: rs1554204122
rs1554204122
1 1.000 0.040 5 177280700 missense variant T/A snv 0.700 0
dbSNP: rs1554204921
rs1554204921
1 1.000 0.040 5 177283797 missense variant T/C snv 0.700 0
dbSNP: rs1554206783
rs1554206783
1 1.000 0.040 5 177292023 stop gained C/T snv 0.700 0
dbSNP: rs1554206836
rs1554206836
1 1.000 0.040 5 177292131 frameshift variant -/G delins 0.700 0
dbSNP: rs1554207316
rs1554207316
1 1.000 0.040 5 177293981 missense variant C/T snv 0.700 0