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: rs12207488
rs12207488
SYCP2L ; LOC101928191
1 6 10952103 intron variant G/A snv 0.19 0.700 1.000 1 2011 2011
dbSNP: rs12213249
rs12213249
SYCP2L
1 6 10926709 intron variant C/T 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: rs1225717
rs1225717
SYCP2L
1 6 10978007 intron variant A/G;T snv 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: rs1225737
rs1225737
ELOVL2
1 6 10982419 3 prime UTR variant C/T snv 0.59 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: rs1225753
rs1225753
SYCP2L
1 6 10956456 intron variant G/A snv 0.43 0.700 1.000 1 2011 2011
dbSNP: rs12459897
rs12459897 		1 19 31105872 intron variant G/T snv 1.2E-02 0.700 1.000 1 2011 2011
dbSNP: rs12526913
rs12526913 		1 6 11082691 downstream gene variant A/G;T snv 0.700 1.000 1 2011 2011
dbSNP: rs12587311
rs12587311 		1 14 28647489 intergenic variant T/C snv 0.53 0.700 1.000 1 2011 2011
dbSNP: rs1260326
rs1260326
GCKR
81 0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 0.700 1.000 1 2011 2011
dbSNP: rs1260333
rs1260333 		12 0.882 0.160 2 27525757 downstream gene variant A/G snv 0.58 0.700 1.000 1 2011 2011
dbSNP: rs12662634
rs12662634
ELOVL2-AS1
1 6 11073958 intron variant G/A snv 0.17 0.700 1.000 1 2011 2011
dbSNP: rs12665478
rs12665478 		1 6 11080592 downstream gene variant G/A snv 0.41 0.700 1.000 1 2011 2011
dbSNP: rs1321535
rs1321535
ELOVL2-AS1
1 6 11075793 intron variant T/G snv 0.41 0.700 1.000 1 2011 2011
dbSNP: rs1321536
rs1321536
ELOVL2
1 6 11018579 intron variant T/A;G snv 0.700 1.000 1 2011 2011
dbSNP: rs1323739
rs1323739
ELOVL2
1 6 11004328 intron variant C/G;T snv 0.700 1.000 1 2011 2011
dbSNP: rs1330767
rs1330767 		1 13 103408241 intergenic variant C/T snv 0.21 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: rs13966
rs13966
RAB3IL1
1 11 61897520 3 prime UTR variant T/C snv 0.53 0.700 1.000 1 2011 2011
dbSNP: rs149803
rs149803
MYRF ; TMEM258
2 11 61771548 synonymous variant C/G;T snv 0.18 0.700 1.000 1 2011 2011
dbSNP: rs1514178
rs1514178
LOC101926964
1 1 60739797 intron variant T/C snv 1.5E-02 0.700 1.000 1 2011 2011
dbSNP: rs1535
rs1535
FADS2
24 0.752 0.240 11 61830500 intron variant A/G snv 0.31 0.700 1.000 1 2011 2011