Source: ALL
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: rs964184
rs964184
ZPR1
47 0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82 0.800 1.000 1 2012 2012
dbSNP: rs10404486
rs10404486
ZNF600
1 19 52780882 non coding transcript exon variant C/T snv 0.20 0.800 1.000 1 2012 2012
dbSNP: rs4666002
rs4666002
ZNF512
6 0.925 0.120 2 27617773 intron variant G/A;C snv 0.800 1.000 1 2012 2012
dbSNP: rs3117181
rs3117181
TNXB
1 6 32103240 intron variant C/A;G;T snv 0.700 1.000 1 2011 2011
dbSNP: rs174538
rs174538
TMEM258 ; FEN1 ; MIR611
21 0.701 0.440 11 61792609 5 prime UTR variant G/A snv 0.34 0.26 0.700 1.000 1 2011 2011
dbSNP: rs412334
rs412334
TMEM258 ; FEN1 ; MIR611
2 11 61792789 5 prime UTR variant C/T snv 0.10 0.700 1.000 1 2011 2011
dbSNP: rs7102974
rs7102974
TMEM258 ; FEN1 ; MIR611
1 11 61792563 5 prime UTR variant C/T snv 8.5E-03 9.6E-03 0.700 1.000 1 2011 2011
dbSNP: rs695867
rs695867
TMEM258 ; FEN1 ; FADS2 ; MIR611
1 11 61793816 intron variant A/G snv 2.6E-02 0.700 1.000 1 2011 2011
dbSNP: rs102275
rs102275
TMEM258
18 0.827 0.320 11 61790331 non coding transcript exon variant T/C snv 0.47 0.800 1.000 3 2011 2013
dbSNP: rs740006
rs740006
TMEM258
2 11 61790396 3 prime UTR variant T/C snv 7.6E-02 0.700 1.000 1 2011 2011
dbSNP: rs6671200
rs6671200
TLCD4-RWDD3 ; LOC101928118
2 1 95231973 intron variant A/C snv 0.90 0.700 1.000 1 2013 2013
dbSNP: rs10769780
rs10769780
SYT9
1 11 7345864 intron variant T/C snv 0.25 0.800 1.000 1 2012 2012
dbSNP: rs1007323
rs1007323
SYCP2L ; LOC101928191
1 6 10953011 intron variant T/A;G snv 0.700 1.000 1 2011 2011
dbSNP: rs12199131
rs12199131
SYCP2L ; LOC101928191
1 6 10932336 intron variant G/A;T snv 0.700 1.000 1 2011 2011
dbSNP: rs12200867
rs12200867
SYCP2L ; LOC101928191
1 6 10939591 intron variant C/G snv 0.22 0.700 1.000 1 2011 2011
dbSNP: rs12207488
rs12207488
SYCP2L ; LOC101928191
1 6 10952103 intron variant G/A snv 0.19 0.700 1.000 1 2011 2011
dbSNP: rs12214825
rs12214825
SYCP2L ; LOC101928191
1 6 10933145 intron variant C/T snv 0.20 0.700 1.000 1 2011 2011
dbSNP: rs1225736
rs1225736
SYCP2L ; LOC101928191
1 6 10939156 intron variant A/G snv 0.24 0.700 1.000 1 2011 2011
dbSNP: rs1225741
rs1225741
SYCP2L ; LOC101928191
1 6 10952010 intron variant G/A snv 0.39 0.700 1.000 1 2011 2011
dbSNP: rs1225744
rs1225744
SYCP2L ; LOC101928191
1 6 10954307 intron variant C/T snv 0.35 0.700 1.000 1 2011 2011
dbSNP: rs1359159
rs1359159
SYCP2L ; LOC101928191
1 6 10934138 intron variant C/G snv 0.13 0.700 1.000 1 2011 2011
dbSNP: rs1578068
rs1578068
SYCP2L ; LOC101928191
1 6 10937871 intron variant T/G snv 0.24 0.700 1.000 1 2011 2011
dbSNP: rs2327323
rs2327323
SYCP2L ; LOC101928191
1 6 10933580 intron variant C/G snv 0.18 0.700 1.000 1 2011 2011
dbSNP: rs9379969
rs9379969
SYCP2L ; LOC101928191
1 6 10952403 intron variant T/A snv 0.19 0.700 1.000 1 2011 2011
dbSNP: rs9393800
rs9393800
SYCP2L ; LOC101928191
3 6 10951504 intron variant A/G snv 0.20 0.700 1.000 1 2011 2011