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: rs1007323
rs1007323
SYCP2L ; LOC101928191
1 6 10953011 intron variant T/A;G snv 0.700 1.000 1 2011 2011
dbSNP: rs10792320
rs10792320 		1 11 61978819 intergenic variant A/C;T snv 0.700 1.000 1 2011 2011
dbSNP: rs11230815
rs11230815 		2 11 61868654 downstream gene variant G/C;T snv 0.700 1.000 1 2011 2011
dbSNP: rs11667159
rs11667159 		3 19 46291989 intergenic variant C/A;T snv 0.700 1.000 1 2017 2017
dbSNP: rs11671710
rs11671710 		3 19 46288677 regulatory region variant C/G;T snv 0.700 1.000 1 2017 2017
dbSNP: rs12199131
rs12199131
SYCP2L ; LOC101928191
1 6 10932336 intron variant G/A;T snv 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: rs12472274
rs12472274
ILKAP
1 2 238186781 non coding transcript exon variant G/A;T snv 0.800 1.000 1 2012 2012
dbSNP: rs12526913
rs12526913 		1 6 11082691 downstream gene variant A/G;T snv 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: rs149803
rs149803
MYRF ; TMEM258
2 11 61771548 synonymous variant C/G;T snv 0.18 0.700 1.000 1 2011 2011
dbSNP: rs17156426
rs17156426
FADS2
2 11 61841851 intron variant A/G;T snv 0.700 1.000 1 2011 2011
dbSNP: rs174455
rs174455
FADS3
5 1.000 0.080 11 61888645 intron variant G/A;C snv 0.700 1.000 1 2011 2011
dbSNP: rs174476
rs174476
RAB3IL1
2 11 61906646 synonymous variant C/A;G;T snv 0.30 0.700 1.000 1 2011 2011
dbSNP: rs174548
rs174548
FADS1 ; FADS2
17 0.851 0.160 11 61803876 5 prime UTR variant C/G;T snv 0.700 1.000 1 2008 2008
dbSNP: rs174585
rs174585
FADS2
2 11 61844222 intron variant G/A;T snv 0.700 1.000 1 2011 2011
dbSNP: rs174589
rs174589
FADS2
1 11 61848331 intron variant C/G;T snv 0.19 0.700 1.000 1 2011 2011
dbSNP: rs174591
rs174591
FADS2
2 11 61850204 intron variant T/A;G snv 0.700 1.000 1 2011 2011
dbSNP: rs174597
rs174597
FADS2
2 11 61853568 intron variant G/A;C;T snv 0.700 1.000 1 2011 2011
dbSNP: rs174634
rs174634
FADS3 ; MIR6746
2 11 61879915 intron variant G/C;T snv 0.700 1.000 1 2011 2011
dbSNP: rs17764324
rs17764324
FADS2
2 11 61867616 downstream gene variant G/A;T snv 0.700 1.000 1 2011 2011
dbSNP: rs17764592
rs17764592
ELOVL2
1 6 11002911 intron variant A/C;G snv 0.700 1.000 1 2011 2011
dbSNP: rs198428
rs198428
DAGLA
1 11 61722233 intron variant A/G;T snv 0.700 1.000 1 2011 2011
dbSNP: rs2028062
rs2028062 		1 11 61978481 intergenic variant G/A;C snv 0.700 1.000 1 2011 2011