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: rs143747297
rs143747297
1 1.000 6 73482061 missense variant G/A snv 5.6E-05 4.2E-05 0.800 1.000 3 2012 2014
dbSNP: rs201544686
rs201544686
1 1.000 6 73482209 missense variant G/A snv 1.7E-04 2.7E-04 0.700 1.000 3 2013 2018
dbSNP: rs1033653237
rs1033653237
1 1.000 6 73482208 missense variant C/T snv 0.700 0
dbSNP: rs1275100093
rs1275100093
1 1.000 6 73482035 splice region variant T/C;G snv 0.700 0
dbSNP: rs1554148965
rs1554148965
1 1.000 6 73479960 missense variant A/C snv 0.700 0
dbSNP: rs1561954433
rs1561954433
1 1.000 6 73497801 frameshift variant C/- del 0.700 0
dbSNP: rs371179032
rs371179032
1 1.000 6 73479844 missense variant G/A snv 1.2E-05 1.4E-05 0.700 0
dbSNP: rs397518449
rs397518449
1 1.000 6 73497836 frameshift variant -/A delins 0.700 0
dbSNP: rs398122419
rs398122419
1 1.000 6 73480777 missense variant C/T snv 2.4E-05 7.0E-06 0.700 0
dbSNP: rs748152539
rs748152539
1 1.000 6 73482229 missense variant C/T snv 2.0E-05 4.2E-05 0.700 0