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: rs122467169
rs122467169
1 1.000 0.200 X 49251698 missense variant A/C snv 0.800 1.000 6 2000 2011
dbSNP: rs28935477
rs28935477
1 1.000 0.200 X 49251441 missense variant G/A snv 5.5E-06 1.9E-05 0.800 1.000 6 2000 2011
dbSNP: rs886044787
rs886044787
1 1.000 0.200 X 49253155 missense variant G/C snv 0.710 1.000 7 2000 2011
dbSNP: rs122467170
rs122467170
1 1.000 0.200 X 49251480 missense variant C/T snv 0.700 1.000 3 2001 2017
dbSNP: rs886041596
rs886041596
1 1.000 0.200 X 49258295 splice donor variant C/A;G snv 0.700 1.000 2 2001 2001
dbSNP: rs122467171
rs122467171
1 1.000 0.200 X 49255492 inframe deletion CCT/- delins 0.700 0
dbSNP: rs122467172
rs122467172
1 1.000 0.200 X 49251692 missense variant AA/GC mnv 0.700 0
dbSNP: rs122467173
rs122467173
1 1.000 0.200 X 49253200 missense variant A/G snv 0.700 0
dbSNP: rs122467174
rs122467174
1 1.000 0.200 X 49258503 start lost C/T snv 0.700 0
dbSNP: rs122467175
rs122467175
1 1.000 0.200 X 49251711 missense variant A/G snv 0.700 0
dbSNP: rs1557115532
rs1557115532
1 1.000 0.200 X 49251408 missense variant C/T snv 0.700 0
dbSNP: rs1569529565
rs1569529565
1 1.000 0.200 X 49251358 frameshift variant ACA/G delins 0.700 0
dbSNP: rs1569529715
rs1569529715
1 1.000 0.200 X 49255756 missense variant A/C snv 0.700 0
dbSNP: rs782528935
rs782528935
1 1.000 0.200 X 49257447 missense variant G/A;T snv 7.6E-06 0.700 0
dbSNP: rs797045588
rs797045588
1 1.000 0.200 X 49255723 frameshift variant C/- delins 0.700 0
dbSNP: rs1057520529
rs1057520529
5 0.851 0.320 X 49251440 missense variant C/T snv 0.020 1.000 2 2014 2017
dbSNP: rs200554980
rs200554980
1 1.000 0.200 X 49257541 missense variant G/A snv 2.6E-04 2.3E-04 0.010 1.000 1 2018 2018
dbSNP: rs782112916
rs782112916
1 1.000 0.200 X 49251335 stop retained variant C/T snv 3.8E-05 0.010 1.000 1 2017 2017