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: rs10482996
rs10482996
1 21 29492492 intron variant C/T snv 7.6E-02 0.700 1.000 1 2009 2009
dbSNP: rs2000460
rs2000460
1 21 29494804 intron variant A/G snv 0.86 0.700 1.000 1 2009 2009
dbSNP: rs2211887
rs2211887
1 21 29492828 intron variant T/C snv 0.82 0.700 1.000 1 2009 2009
dbSNP: rs2832357
rs2832357
1 21 29491574 intron variant A/G snv 0.12 0.700 1.000 1 2009 2009
dbSNP: rs2832361
rs2832361
1 21 29498804 intron variant C/T snv 6.4E-02 0.700 1.000 1 2009 2009
dbSNP: rs2832367
rs2832367
1 21 29501649 intron variant C/T snv 8.0E-02 0.700 1.000 1 2009 2009
dbSNP: rs963072
rs963072
1 21 29495316 intron variant T/A;C;G snv 0.700 1.000 1 2009 2009
dbSNP: rs963073
rs963073
1 21 29495132 intron variant T/C snv 0.83 0.700 1.000 1 2009 2009
dbSNP: rs980007
rs980007
1 21 29492962 intron variant A/G snv 0.83 0.700 1.000 1 2009 2009