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: rs1505637
rs1505637 		1 9 78582032 intergenic variant G/A snv 0.72 0.700 1.000 1 2012 2012
dbSNP: rs1505640
rs1505640 		1 9 78580130 intergenic variant T/A;C snv 0.700 1.000 1 2012 2012
dbSNP: rs1505642
rs1505642 		1 9 78579468 intergenic variant G/A snv 0.70 0.700 1.000 1 2012 2012
dbSNP: rs1539878
rs1539878
KATNAL2
1 18 46943041 intron variant T/C snv 0.53 0.700 1.000 1 2012 2012
dbSNP: rs16902538
rs16902538
LINC01949 ; LOC101929380
1 5 87121196 intron variant C/T snv 0.23 0.700 1.000 1 2012 2012
dbSNP: rs17018311
rs17018311
INTS7
2 1.000 0.040 1 211981666 intron variant T/C snv 2.7E-02 0.700 1.000 1 2012 2012
dbSNP: rs17591778
rs17591778
LINC01949 ; LOC101929380
1 5 87124575 intron variant G/A snv 0.25 0.700 1.000 1 2012 2012
dbSNP: rs17629700
rs17629700
LINC01949 ; LOC101929380
1 5 87124691 intron variant C/A;T snv 0.700 1.000 1 2012 2012
dbSNP: rs17629760
rs17629760
LINC01949 ; LOC101929380
1 5 87128242 intron variant G/A snv 0.23 0.700 1.000 1 2012 2012
dbSNP: rs1985671
rs1985671
FBLN1
2 1.000 0.040 22 45566024 intron variant G/T snv 0.65 0.700 1.000 1 2012 2012
dbSNP: rs2032215
rs2032215
PIAS2
1 18 46859048 intron variant A/C snv 0.57 0.700 1.000 1 2012 2012
dbSNP: rs2156050
rs2156050
PIAS2
1 18 46875910 intron variant A/G snv 0.53 0.700 1.000 1 2012 2012
dbSNP: rs2246877
rs2246877
KATNAL2
1 18 47050634 intron variant A/G snv 0.34 0.700 1.000 1 2012 2012
dbSNP: rs2247578
rs2247578
SKOR2
1 18 47218685 intron variant A/G;T snv 0.700 1.000 1 2012 2012
dbSNP: rs2247777
rs2247777
SKOR2
1 18 47220368 intron variant C/G snv 0.54 0.700 1.000 1 2012 2012
dbSNP: rs2510444
rs2510444 		1 18 46796886 intron variant G/T snv 0.51 0.700 1.000 1 2012 2012
dbSNP: rs2544698
rs2544698
LOC101929380
1 5 87159014 intergenic variant C/G;T snv 0.700 1.000 1 2012 2012
dbSNP: rs2571034
rs2571034
KATNAL2
1 18 47052194 intron variant A/G snv 0.40 0.700 1.000 1 2012 2012
dbSNP: rs2576037
rs2576037
KATNAL2
1 18 47059049 intron variant C/T snv 0.41 0.700 1.000 1 2012 2012
dbSNP: rs2668778
rs2668778
SKOR2
1 18 47218814 intron variant A/C snv 0.56 0.700 1.000 1 2012 2012
dbSNP: rs2684814
rs2684814
SKOR2
1 18 47227732 intron variant T/C snv 0.58 0.700 1.000 1 2012 2012
dbSNP: rs3765066
rs3765066
SCAMP2
1 15 74848513 non coding transcript exon variant G/A snv 0.48 0.700 1.000 1 2012 2012
dbSNP: rs4141503
rs4141503
LINC01949 ; LOC101929380
1 5 87128859 intron variant C/T snv 0.23 0.700 1.000 1 2012 2012
dbSNP: rs416350
rs416350
LINC02384
2 1.000 0.040 12 68385633 intron variant G/A;T snv 0.700 1.000 1 2012 2012
dbSNP: rs4890341
rs4890341
PIAS2
1 18 46887405 intron variant T/C;G snv 0.700 1.000 1 2012 2012