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: 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: rs138572223
rs138572223 		2 18 50446052 intergenic variant A/G snv 5.7E-03 0.700 1.000 1 2017 2017
dbSNP: rs139368489
rs139368489 		2 18 50502045 intergenic variant T/C snv 5.8E-03 0.700 1.000 1 2017 2017
dbSNP: rs13966
rs13966
RAB3IL1
1 11 61897520 3 prime UTR variant T/C snv 0.53 0.700 1.000 1 2011 2011
dbSNP: rs141332218
rs141332218 		3 19 46293976 upstream gene variant T/C snv 0.12 0.700 1.000 1 2017 2017
dbSNP: rs1424760
rs1424760 		1 2 162925277 intergenic variant C/T snv 0.52 0.800 1.000 1 2012 2012
dbSNP: rs142815467
rs142815467 		3 19 46291277 intergenic variant -/T delins 0.12 0.700 1.000 1 2017 2017
dbSNP: rs146524044
rs146524044
MYO5B
2 18 50057046 intron variant A/C snv 1.0E-03 0.700 1.000 1 2017 2017
dbSNP: rs149803
rs149803
MYRF ; TMEM258
2 11 61771548 synonymous variant C/G;T snv 0.18 0.700 1.000 1 2011 2011
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: 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: rs16832011
rs16832011
LCT
1 2 135787729 downstream gene variant A/G snv 5.1E-02 0.700 1.000 1 2011 2011
dbSNP: rs1692120
rs1692120 		1 11 61650000 downstream gene variant G/A snv 0.43 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: rs174449
rs174449 		2 11 61872907 downstream gene variant G/A snv 0.54 0.700 1.000 1 2011 2011