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: rs10883371
rs10883371
NKX2-3 ; LINC01475
1 1.000 0.040 10 99532698 upstream gene variant C/A snv 0.54 0.700 1.000 1 2013 2013
dbSNP: rs10905718
rs10905718 		1 1.000 0.040 10 6072893 upstream gene variant A/G snv 0.25 0.700 1.000 1 2011 2011
dbSNP: rs12479056
rs12479056
PUS10
1 1.000 0.040 2 60948177 synonymous variant T/C snv 0.56 0.62 0.700 1.000 1 2013 2013
dbSNP: rs13132245
rs13132245 		1 1.000 0.040 4 122128437 intergenic variant A/G snv 0.11 0.700 1.000 1 2012 2012
dbSNP: rs13191240
rs13191240
ADGRB3
1 1.000 0.040 6 68965567 intron variant T/C snv 4.5E-02 0.010 1.000 1 2017 2017
dbSNP: rs17683107
rs17683107
GAS7
1 1.000 0.040 17 9921085 intron variant G/A snv 0.13 0.700 1.000 1 2011 2011
dbSNP: rs2844559
rs2844559 		1 1.000 0.040 6 31372298 intron variant C/T snv 8.0E-02 0.700 1.000 1 2010 2010
dbSNP: rs3134883
rs3134883
IL2RA
1 1.000 0.040 10 6058762 intron variant G/A snv 0.23 0.700 1.000 1 2011 2011
dbSNP: rs34762726
rs34762726
BSN
1 1.000 0.040 3 49651777 missense variant G/A snv 0.27 0.28 0.700 1.000 1 2013 2013
dbSNP: rs415595
rs415595
TNP2 ; RMI2 ; LOC105371082
1 1.000 0.040 16 11269835 intron variant A/G snv 0.46 0.700 1.000 1 2013 2013
dbSNP: rs4391646
rs4391646
LOC112268276
1 1.000 0.040 1 166208147 intron variant T/C snv 0.22 0.700 1.000 1 2011 2011
dbSNP: rs633683
rs633683
PHLDB1
1 1.000 0.040 11 118634025 non coding transcript exon variant T/C snv 0.58 0.700 1.000 1 2013 2013
dbSNP: rs6678400
rs6678400
LOC112268276
1 1.000 0.040 1 166208523 intron variant G/T snv 0.22 0.700 1.000 1 2011 2011
dbSNP: rs6971637
rs6971637
LOC101927243
1 1.000 0.040 7 77425403 non coding transcript exon variant C/T snv 7.1E-03 0.700 1.000 1 2011 2011
dbSNP: rs7791854
rs7791854 		1 1.000 0.040 7 77427905 downstream gene variant C/T snv 3.3E-03 0.700 1.000 1 2011 2011
dbSNP: rs9686714
rs9686714
WWC1
1 1.000 0.040 5 168426269 intron variant T/C snv 0.13 0.010 1.000 1 2017 2017
dbSNP: rs13140464
rs13140464 		2 0.925 0.040 4 122578590 regulatory region variant G/T snv 0.10 0.700 1.000 1 2013 2013
dbSNP: rs1788097
rs1788097
CD226
2 0.925 0.040 18 69876452 intron variant C/T snv 0.56 0.700 1.000 1 2013 2013
dbSNP: rs35730843
rs35730843
POLR2G
2 0.925 0.080 11 62760162 upstream gene variant A/C;G snv 0.12 0.010 1.000 1 2017 2017
dbSNP: rs3822659
rs3822659
WWC1
2 0.925 0.080 5 168431367 missense variant T/G snv 8.7E-02 0.12 0.010 1.000 1 2017 2017
dbSNP: rs4147359
rs4147359 		2 0.925 0.040 10 6066476 upstream gene variant G/A snv 0.33 0.700 1.000 1 2013 2013
dbSNP: rs4620530
rs4620530
CHRM3 ; CHRM3-AS1
2 0.925 0.080 1 239900521 intron variant T/G snv 0.44 0.010 1.000 1 2020 2020
dbSNP: rs56258221
rs56258221
LOC105377891
2 0.925 0.040 6 90320722 intron variant T/C snv 0.13 0.700 1.000 1 2013 2013
dbSNP: rs60652743
rs60652743
PRKD2
2 0.925 0.040 19 46702450 intron variant A/G snv 0.16 0.700 1.000 1 2013 2013
dbSNP: rs6720394
rs6720394
MIR4435-2HG
2 0.925 0.040 2 111231795 intron variant T/G snv 0.11 0.700 1.000 1 2011 2011