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: rs10039217
rs10039217 		1 5 175751872 intergenic variant A/G snv 4.6E-02 0.800 1.000 1 2012 2012
dbSNP: rs11662748
rs11662748
MIR3976HG
1 18 5762619 splice region variant G/A snv 0.17 0.800 1.000 1 2012 2012
dbSNP: rs13036722
rs13036722
DEFB128
1 20 187379 downstream gene variant T/C snv 0.16 0.800 1.000 1 2012 2012
dbSNP: rs7665957
rs7665957
LOC105374492
1 4 12497263 intergenic variant C/G;T snv 0.800 1.000 1 2012 2012
dbSNP: rs8037818
rs8037818
ARHGAP11A ; ARHGAP11A-SCG5
1 15 32635275 intron variant C/T snv 0.79 0.800 1.000 1 2012 2012
dbSNP: rs10018902
rs10018902 		2 4 120941346 intergenic variant G/A;T snv 0.700 1.000 1 2012 2012
dbSNP: rs10097849
rs10097849
SGCZ
1 8 14672342 intron variant T/G snv 0.55 0.700 1.000 1 2012 2012
dbSNP: rs10107366
rs10107366 		1 8 98101459 downstream gene variant T/C snv 2.0E-02 0.700 1.000 1 2012 2012
dbSNP: rs10131141
rs10131141
LOC105370397 ; LOC107984671
1 14 20793574 intergenic variant C/T snv 0.62 0.700 1.000 1 2012 2012
dbSNP: rs10198552
rs10198552
ACMSD ; CCNT2-AS1
2 2 134842306 intron variant T/C snv 6.2E-02 0.700 1.000 1 2012 2012
dbSNP: rs1020410
rs1020410 		1 2 175919410 downstream gene variant T/C snv 0.34 0.700 1.000 1 2012 2012
dbSNP: rs10502386
rs10502386 		2 18 8966146 intergenic variant G/T snv 0.39 0.700 1.000 1 2012 2012
dbSNP: rs10504576
rs10504576
GDAP1
1 8 74354444 intron variant A/G snv 0.47 0.700 1.000 1 2007 2007
dbSNP: rs10511378
rs10511378 		1 3 118443776 intron variant T/C snv 0.16 0.700 1.000 1 2012 2012
dbSNP: rs1053221
rs1053221
KMO ; OPN3
1 1 241592265 3 prime UTR variant T/C snv 0.13 0.700 1.000 1 2012 2012
dbSNP: rs1056513
rs1056513
PATJ
3 1 61914626 missense variant G/A;C snv 0.57; 8.0E-06 0.700 1.000 1 2012 2012
dbSNP: rs10739496
rs10739496
PTCSC2
1 9 97790277 intron variant C/G;T snv 0.700 1.000 1 2012 2012
dbSNP: rs10744816
rs10744816 		2 12 114276461 regulatory region variant T/C snv 0.39 0.700 1.000 1 2012 2012
dbSNP: rs10747502
rs10747502
LOC100129620
2 1.000 0.040 1 99058491 intron variant A/G snv 0.86 0.700 1.000 1 2012 2012
dbSNP: rs10759944
rs10759944
PTCSC2
4 0.925 0.080 9 97794690 intron variant A/G snv 0.72 0.700 1.000 1 2012 2012
dbSNP: rs10818090
rs10818090
PTCSC2
1 9 97799204 intron variant C/T snv 0.73 0.700 1.000 1 2012 2012
dbSNP: rs10830963
rs10830963
MTNR1B
27 0.776 0.400 11 92975544 intron variant C/G snv 0.22 0.700 1.000 1 2012 2012
dbSNP: rs1084004
rs1084004
SLC29A3
1 10 71362188 synonymous variant T/C;G snv 0.83 0.700 1.000 1 2012 2012
dbSNP: rs10906142
rs10906142
CAMK1D
1 10 12396784 intron variant G/A snv 0.29 0.700 1.000 1 2012 2012
dbSNP: rs10983700
rs10983700
PTCSC2
2 1.000 0.080 9 97775173 intron variant T/A;C snv 0.700 1.000 1 2012 2012