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: rs1000668
rs1000668
TMC1
1 9 72790943 intron variant T/A;G snv 0.700 1.000 1 2012 2012
dbSNP: rs10186527
rs10186527
FLACC1
1 2 201335852 intron variant C/T snv 0.54 0.700 1.000 1 2012 2012
dbSNP: rs10191793
rs10191793
ST6GAL2
1 2 106809420 intron variant A/G snv 0.21 0.700 1.000 1 2012 2012
dbSNP: rs10197246
rs10197246
FLACC1
1 2 201340018 intron variant T/C snv 0.72 0.700 1.000 1 2012 2012
dbSNP: rs10201587
rs10201587
FLACC1
1 2 201338068 intron variant A/G snv 0.47 0.700 1.000 1 2012 2012
dbSNP: rs10454127
rs10454127
FLACC1
1 2 201347651 intron variant G/A;T snv 0.700 1.000 1 2012 2012
dbSNP: rs10502995
rs10502995 		1 18 55138645 regulatory region variant G/A snv 0.20 0.700 1.000 1 2012 2012
dbSNP: rs11051196
rs11051196
TSPAN11
1 12 30980130 intron variant C/T snv 0.27 0.700 1.000 1 2012 2012
dbSNP: rs11065783
rs11065783
LINC01405 ; LOC105369980
1 12 110958445 non coding transcript exon variant A/G snv 1.9E-02 0.700 1.000 1 2010 2010
dbSNP: rs11254327
rs11254327
CUBN
1 10 17006709 intron variant C/T snv 0.40 0.700 1.000 1 2012 2012
dbSNP: rs11776675
rs11776675
CDH17
1 8 94163787 intron variant T/C snv 0.23 0.700 1.000 1 2012 2012
dbSNP: rs11843987
rs11843987
TFDP1
1 13 113589954 intron variant A/G snv 9.1E-02 0.700 1.000 1 2012 2012
dbSNP: rs11898821
rs11898821
FLACC1
1 2 201334965 intron variant T/C snv 0.46 0.700 1.000 1 2012 2012
dbSNP: rs11972901
rs11972901 		1 7 85966605 intergenic variant A/G snv 0.47 0.700 1.000 1 2012 2012
dbSNP: rs12438490
rs12438490
OCA2
1 15 28015163 intron variant C/T snv 7.3E-02 0.700 1.000 1 2012 2012
dbSNP: rs1323135
rs1323135
FKBP1A ; SDCBP2-AS1 ; FKBP1A-SDCBP2
1 20 1377208 non coding transcript exon variant G/C;T snv 0.700 1.000 1 2012 2012
dbSNP: rs1346291
rs1346291
LOC105375925
1 8 81339729 regulatory region variant A/G snv 0.78 0.700 1.000 1 2010 2010
dbSNP: rs1453029
rs1453029 		1 18 41000207 intergenic variant T/C snv 7.0E-02 0.700 1.000 1 2012 2012
dbSNP: rs1548418
rs1548418
STEAP1B
1 7 22685795 intron variant C/A snv 0.89 0.700 1.000 1 2012 2012
dbSNP: rs1570477
rs1570477
KANK1
1 9 657340 intron variant G/A snv 0.63 0.700 1.000 1 2012 2012
dbSNP: rs16901549
rs16901549
PCAT1 ; LOC105375751
1 8 126583939 intron variant G/T snv 8.6E-03 0.700 1.000 1 2012 2012
dbSNP: rs1737076
rs1737076 		1 6 29757544 intron variant A/G snv 0.45 0.700 1.000 1 2012 2012
dbSNP: rs17450420
rs17450420 		1 13 104386796 intergenic variant A/G snv 5.9E-02 0.800 1.000 1 2012 2012
dbSNP: rs2080304
rs2080304
FLACC1
1 2 201321699 intron variant G/C snv 0.59 0.700 1.000 1 2012 2012
dbSNP: rs2110690
rs2110690
FLACC1
1 2 201320409 intron variant A/G snv 0.42 0.700 1.000 1 2012 2012