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: rs9998785
rs9998785
EXOSC9
1 4 121807810 non coding transcript exon variant A/T snv 0.29 0.700 1.000 1 2012 2012
dbSNP: rs9995319
rs9995319
BBS7
2 4 121849522 intron variant G/C snv 0.29 0.700 1.000 1 2012 2012
dbSNP: rs9990333
rs9990333 		4 3 196100334 intergenic variant C/T snv 0.42 0.700 1.000 1 2012 2012
dbSNP: rs9972882
rs9972882
STARD3
4 0.925 0.080 17 39651445 intron variant A/C snv 0.66 0.700 1.000 1 2012 2012
dbSNP: rs9967849
rs9967849
MIR4432HG
3 2 60382339 intron variant C/T snv 0.33 0.700 1.000 1 2012 2012
dbSNP: rs9963843
rs9963843
C18orf25
1 18 46262655 intron variant C/A;T snv 0.700 1.000 1 2012 2012
dbSNP: rs9963153
rs9963153
C18orf25
1 18 46260101 intron variant T/C snv 0.72 0.700 1.000 1 2012 2012
dbSNP: rs9959905
rs9959905
C18orf25
1 18 46231084 intron variant A/G;T snv 0.700 1.000 1 2012 2012
dbSNP: rs9959813
rs9959813
C18orf25
1 18 46261119 intron variant A/G snv 0.74 0.700 1.000 1 2012 2012
dbSNP: rs99595
rs99595 		1 20 57414752 regulatory region variant C/G;T snv 0.700 1.000 1 2012 2012
dbSNP: rs995716
rs995716 		1 4 54500464 intergenic variant G/C snv 0.37 0.700 1.000 1 2012 2012
dbSNP: rs9956574
rs9956574
C18orf25
1 18 46202237 intron variant C/T snv 0.72 0.700 1.000 1 2012 2012
dbSNP: rs9955853
rs9955853
C18orf25
1 18 46249689 intron variant C/T snv 0.43 0.700 1.000 1 2012 2012
dbSNP: rs9955008
rs9955008 		1 18 46078922 upstream gene variant G/A snv 0.59 0.700 1.000 1 2012 2012
dbSNP: rs9952469
rs9952469
C18orf25
1 18 46232044 3 prime UTR variant T/C snv 0.65 0.700 1.000 1 2012 2012
dbSNP: rs9950234
rs9950234
PSTPIP2
1 18 46073234 upstream gene variant T/C snv 0.59 0.700 1.000 1 2012 2012
dbSNP: rs9949494
rs9949494
C18orf25
1 18 46231334 intron variant T/C snv 0.61 0.700 1.000 1 2012 2012
dbSNP: rs9947316
rs9947316
C18orf25
1 18 46197865 intron variant T/A;G snv 0.700 1.000 1 2012 2012
dbSNP: rs9945783
rs9945783
C18orf25
1 18 46202294 intron variant T/C snv 0.61 0.700 1.000 1 2012 2012
dbSNP: rs9944836
rs9944836
C18orf25
1 18 46251414 intron variant A/G;T snv 0.700 1.000 1 2012 2012
dbSNP: rs9944767
rs9944767
C18orf25
1 18 46251091 intron variant G/A snv 0.74 0.700 1.000 1 2012 2012
dbSNP: rs9944411
rs9944411
FBXL20
2 17 39327346 intron variant T/C snv 0.32 0.700 1.000 1 2012 2012
dbSNP: rs994379
rs994379 		1 6 26305179 intergenic variant G/C snv 0.54 0.700 1.000 1 2012 2012
dbSNP: rs9938020
rs9938020
NFATC3
1 16 68217881 3 prime UTR variant C/G snv 0.21 0.700 1.000 1 2012 2012
dbSNP: rs9933309
rs9933309
PIEZO1
1 16 88778524 intron variant T/C snv 0.72 0.700 1.000 1 2012 2012