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: rs10569394
rs10569394
1 6 31272468 intron variant -/TC delins 0.700 1.000 1 2018 2018
dbSNP: rs1140404
rs1140404
1 6 31356750 missense variant T/C;G snv 0.700 1.000 1 2018 2018
dbSNP: rs116576188
rs116576188
1 6 31328592 intron variant A/C snv 1.2E-02 0.700 1.000 1 2018 2018
dbSNP: rs1634738
rs1634738
1 6 31316290 intron variant G/A;T snv 0.700 1.000 1 2018 2018
dbSNP: rs2524139
rs2524139
2 1.000 0.040 6 31296356 intron variant G/C;T snv 0.700 1.000 1 2018 2018
dbSNP: rs2524142
rs2524142
2 1.000 0.040 6 31295745 intron variant C/A;G snv 0.700 1.000 1 2018 2018
dbSNP: rs2524143
rs2524143
2 1.000 0.040 6 31295733 intron variant T/C snv 0.81 0.700 1.000 1 2018 2018
dbSNP: rs41552714
rs41552714
1 6 31356979 missense variant G/A snv 3.6E-02 7.5E-02 0.700 1.000 1 2018 2018
dbSNP: rs558163186
rs558163186
1 6 31285529 intron variant AA/-;A;AAA;AAAA delins 0.700 1.000 1 2018 2018
dbSNP: rs568630420
rs568630420
1 6 31347810 intron variant G/T snv 0.700 1.000 1 2018 2018
dbSNP: rs6457374
rs6457374
9 0.851 0.200 6 31304484 intron variant C/T snv 0.81 0.700 1.000 1 2018 2018
dbSNP: rs7750963
rs7750963
2 1.000 0.080 6 31303790 intron variant A/G snv 0.80 0.700 1.000 1 2018 2018
dbSNP: rs9264845
rs9264845
1 6 31303299 intron variant G/C snv 0.700 1.000 1 2018 2018
dbSNP: rs9265503
rs9265503
1 6 31329803 intron variant C/T snv 0.700 1.000 1 2018 2018