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: rs1555639411
rs1555639411
10 0.790 0.360 17 67894102 frameshift variant -/G delins 0.700 1.000 1 2017 2017
dbSNP: rs121434341
rs121434341
10 0.807 0.360 8 60855993 missense variant C/A;T snv 0.700 0
dbSNP: rs1554603293
rs1554603293
17 0.752 0.320 8 60849154 missense variant G/A snv 0.700 0
dbSNP: rs367557471
rs367557471
4 1.000 0.120 8 60822055 stop gained C/A;T snv 5.2E-05 7.0E-05 0.700 0
dbSNP: rs104894110
rs104894110
8 0.776 0.280 9 97854108 missense variant C/T snv 0.010 1.000 1 1998 1998
dbSNP: rs1353175955
rs1353175955
2 0.925 0.200 19 38290170 missense variant G/A snv 4.0E-06 0.010 1.000 1 2017 2017
dbSNP: rs1474322770
rs1474322770
5 0.827 0.240 14 36519251 missense variant G/A snv 0.010 1.000 1 1998 1998