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: rs10013443
rs10013443
PALLD
1 1.000 0.080 4 168685769 intron variant T/C snv 3.4E-02 0.700 1.000 1 2009 2009
dbSNP: rs10024442
rs10024442
TMEM131L
1 1.000 0.080 4 153570903 intron variant T/G snv 0.13 0.700 1.000 1 2009 2009
dbSNP: rs10032741
rs10032741 		1 1.000 0.080 4 44958427 intergenic variant T/A;C snv 0.700 1.000 1 2009 2009
dbSNP: rs10035360
rs10035360 		1 1.000 0.080 5 34604531 regulatory region variant C/T snv 0.19 0.700 1.000 1 2009 2009
dbSNP: rs10045595
rs10045595
TENM2
1 1.000 0.080 5 167802999 intron variant T/G snv 0.36 0.700 1.000 1 2009 2009
dbSNP: rs10091183
rs10091183 		1 1.000 0.080 8 33215980 regulatory region variant A/G snv 4.6E-02 0.700 1.000 1 2009 2009
dbSNP: rs10094069
rs10094069
CSMD3
1 1.000 0.080 8 113022302 intron variant C/T snv 0.59 0.700 1.000 1 2009 2009
dbSNP: rs1009449
rs1009449
LOC105376617
1 1.000 0.080 11 33684620 intron variant A/G snv 4.2E-03 0.700 1.000 1 2009 2009
dbSNP: rs1011356
rs1011356 		1 1.000 0.080 14 76678871 intron variant C/A;G snv 0.700 1.000 1 2009 2009
dbSNP: rs10160659
rs10160659
DCHS1
1 1.000 0.080 11 6644463 intron variant A/C snv 5.5E-02 0.700 1.000 1 2009 2009
dbSNP: rs10200800
rs10200800
KCNE4
1 1.000 0.080 2 223088118 intron variant T/C snv 0.75 0.700 1.000 1 2009 2009
dbSNP: rs10226621
rs10226621
SDK1
1 1.000 0.080 7 4068008 intron variant A/C;G snv 0.700 1.000 1 2009 2009
dbSNP: rs10240026
rs10240026
LOC105379749
1 1.000 0.080 7 142491501 upstream gene variant A/T snv 6.8E-02 0.700 1.000 1 2009 2009
dbSNP: rs10418441
rs10418441
COLGALT1
1 1.000 0.080 19 17569292 intron variant C/A;T snv 0.700 1.000 1 2009 2009
dbSNP: rs10487465
rs10487465
GRM8
1 1.000 0.080 7 127056727 intron variant T/C snv 7.9E-02 0.700 1.000 1 2009 2009
dbSNP: rs10490165
rs10490165
NRXN1
1 1.000 0.080 2 50961428 intron variant T/A;C snv 0.700 1.000 1 2009 2009
dbSNP: rs10775354
rs10775354
RBFOX1
1 1.000 0.080 16 6757689 intron variant A/C;T snv 0.700 1.000 1 2009 2009
dbSNP: rs10780661
rs10780661
SLC28A3
1 1.000 0.080 9 84311392 intron variant A/G;T snv 0.700 1.000 1 2009 2009
dbSNP: rs10915020
rs10915020 		1 1.000 0.080 1 34692115 intergenic variant T/A snv 0.10 0.700 1.000 1 2013 2013
dbSNP: rs10918931
rs10918931 		1 1.000 0.080 1 168592853 intergenic variant T/C snv 0.61 0.700 1.000 1 2009 2009
dbSNP: rs10944489
rs10944489
MAP3K7
1 1.000 0.080 6 90554374 intron variant G/A snv 3.6E-02 0.700 1.000 1 2009 2009
dbSNP: rs10956273
rs10956273
LINC00861
1 1.000 0.080 8 125953914 non coding transcript exon variant A/G snv 6.9E-02 0.700 1.000 1 2009 2009
dbSNP: rs10974284
rs10974284
GLIS3
1 1.000 0.080 9 4028700 intron variant T/C snv 1.2E-02 0.700 1.000 1 2009 2009
dbSNP: rs11030600
rs11030600 		1 1.000 0.080 11 29174695 intron variant T/G snv 8.9E-02 0.700 1.000 1 2009 2009
dbSNP: rs1105358
rs1105358
C9orf92
1 1.000 0.080 9 16265821 intron variant G/C snv 0.10 0.700 1.000 1 2009 2009