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: rs1555360362
rs1555360362
1 1.000 14 75963326 frameshift variant A/- delins 0.700 1.000 4 1992 2015
dbSNP: rs796051885
rs796051885
2 0.925 14 75963344 missense variant G/A snv 0.700 1.000 3 2014 2015
dbSNP: rs1555360883
rs1555360883
1 1.000 14 75971719 splice acceptor variant C/G snv 0.700 1.000 1 2015 2015
dbSNP: rs1566682530
rs1566682530
1 1.000 14 75971256 splice acceptor variant C/G snv 0.700 1.000 1 2015 2015
dbSNP: rs1057523647
rs1057523647
1 1.000 14 75971629 stop gained G/A snv 0.700 0
dbSNP: rs1060502826
rs1060502826
1 1.000 14 75963358 frameshift variant CC/- delins 0.700 0
dbSNP: rs1060502827
rs1060502827
1 1.000 14 75960969 stop gained G/A;C snv 4.0E-06 0.700 0
dbSNP: rs1555360222
rs1555360222
1 1.000 14 75961014 stop gained C/T snv 0.700 0
dbSNP: rs1555360229
rs1555360229
2 0.925 14 75961030 stop gained G/A snv 0.700 0
dbSNP: rs587777617
rs587777617
2 0.925 14 75963343 missense variant C/T snv 0.700 0