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: rs1225753
rs1225753
SYCP2L
1 6 10956456 intron variant G/A snv 0.43 0.700 1.000 1 2011 2011
dbSNP: rs12423247
rs12423247 		1 12 96464584 intron variant A/T snv 9.2E-02 0.800 1.000 1 2012 2012
dbSNP: rs12459897
rs12459897 		1 19 31105872 intron variant G/T snv 1.2E-02 0.700 1.000 1 2011 2011
dbSNP: rs12529874
rs12529874 		2 6 98014625 intron variant G/A snv 2.6E-02 0.700 1.000 1 2013 2013
dbSNP: rs12662634
rs12662634
ELOVL2-AS1
1 6 11073958 intron variant G/A snv 0.17 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: rs1359159
rs1359159
SYCP2L ; LOC101928191
1 6 10934138 intron variant C/G snv 0.13 0.700 1.000 1 2011 2011
dbSNP: rs146524044
rs146524044
MYO5B
2 18 50057046 intron variant A/C snv 1.0E-03 0.700 1.000 1 2017 2017
dbSNP: rs151159962
rs151159962
SKA1
2 18 50386938 intron variant T/C snv 1.3E-03 0.700 1.000 1 2017 2017
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
dbSNP: rs1570069
rs1570069
ELOVL2
1 6 11017592 intron variant A/G snv 0.54 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: rs17148090
rs17148090
DLG2
1 11 85306432 intron variant A/C;G snv 7.4E-02 0.800 1.000 1 2012 2012
dbSNP: rs17156426
rs17156426
FADS2
2 11 61841851 intron variant A/G;T snv 0.700 1.000 1 2011 2011
dbSNP: rs17156442
rs17156442
FADS2
2 11 61846551 intron variant C/T snv 0.11 0.700 1.000 1 2011 2011
dbSNP: rs174450
rs174450
FADS3
3 1.000 0.080 11 61874070 intron variant G/T snv 0.44 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: rs174456
rs174456
FADS3
2 11 61888710 intron variant C/A snv 0.59 0.700 1.000 1 2011 2011
dbSNP: rs174464
rs174464
FADS3
2 11 61890454 intron variant A/G snv 0.59 0.700 1.000 1 2011 2011
dbSNP: rs174469
rs174469
RAB3IL1
1 11 61899971 intron variant C/T snv 0.14 0.700 1.000 1 2011 2011
dbSNP: rs174472
rs174472
RAB3IL1
2 11 61904484 intron variant A/G snv 0.41 0.700 1.000 1 2011 2011
dbSNP: rs174478
rs174478
RAB3IL1
2 11 61911104 intron variant T/G snv 0.31 0.700 1.000 1 2011 2011