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: rs4733613
rs4733613 		1 1.000 0.080 8 128587032 intergenic variant C/G snv 0.86 0.700 1.000 2 2016 2018
dbSNP: rs10835920
rs10835920 		1 1.000 0.080 11 32468118 intergenic variant C/T snv 0.50 0.700 1.000 1 2018 2018
dbSNP: rs10850382
rs10850382
LOC107984437
1 1.000 0.080 12 114776743 downstream gene variant C/T snv 0.26 0.700 1.000 1 2018 2018
dbSNP: rs1129506
rs1129506
EVI2A ; NF1
1 1.000 0.080 17 31319014 missense variant G/A;C snv 0.59; 6.0E-05 0.700 1.000 1 2018 2018
dbSNP: rs113998067
rs113998067 		1 1.000 0.080 1 37607755 downstream gene variant T/C snv 3.3E-02 0.700 1.000 1 2018 2018
dbSNP: rs11583244
rs11583244 		1 1.000 0.080 1 225764772 regulatory region variant C/T snv 0.35 0.700 1.000 1 2018 2018
dbSNP: rs11657964
rs11657964
HNF1B
1 1.000 0.080 17 37740776 intron variant G/A snv 0.42 0.700 1.000 1 2011 2011
dbSNP: rs117280150
rs117280150 		1 1.000 0.080 8 14014030 intergenic variant T/G snv 2.3E-02 0.700 1.000 1 2018 2018
dbSNP: rs117610694
rs117610694
FCHSD2
1 1.000 0.080 11 73070209 intron variant C/T snv 9.6E-03 0.700 1.000 1 2018 2018
dbSNP: rs11841589
rs11841589 		1 1.000 0.080 13 73240754 intergenic variant G/T snv 0.31 0.700 1.000 1 2016 2016
dbSNP: rs12184995
rs12184995
LINC02331 ; LOC105370504
1 1.000 0.080 14 53759970 intron variant A/G snv 0.83 0.700 1.000 1 2018 2018
dbSNP: rs13328298
rs13328298
LINC02523 ; LOC105377986
1 1.000 0.080 6 125695434 intron variant G/A;C snv 0.700 1.000 1 2016 2016
dbSNP: rs142459060
rs142459060
EXT1
1 1.000 0.080 8 117816659 intron variant T/C snv 2.3E-02 0.700 1.000 1 2018 2018
dbSNP: rs145505949
rs145505949
LINC02451
1 1.000 0.080 12 42656220 intron variant C/T snv 9.3E-02 0.700 1.000 1 2018 2018
dbSNP: rs148261157
rs148261157 		1 1.000 0.080 2 60670444 intergenic variant G/A snv 3.9E-02 0.700 1.000 1 2018 2018
dbSNP: rs1677893
rs1677893
NAV3
1 1.000 0.080 12 77944606 intron variant A/T snv 0.48 0.700 1.000 1 2018 2018
dbSNP: rs1679014
rs1679014 		1 1.000 0.080 9 22207038 intron variant T/A;C snv 0.700 1.000 1 2018 2018
dbSNP: rs17232730
rs17232730
LINC00824
1 1.000 0.080 8 128525500 intron variant G/C snv 9.8E-02 0.700 1.000 1 2016 2016
dbSNP: rs17761446
rs17761446
CDKN2B-AS1
1 1.000 0.080 9 22118103 non coding transcript exon variant T/G snv 2.0E-02 0.010 1.000 1 2016 2016
dbSNP: rs1923357
rs1923357
PTPRD
1 1.000 0.080 9 10266786 intron variant C/T snv 0.72 0.700 1.000 1 2018 2018
dbSNP: rs2070833
rs2070833
BRCA1
1 1.000 0.080 17 43090832 intron variant G/T snv 2.1E-02 0.010 1.000 1 2015 2015
dbSNP: rs2498796
rs2498796
AKT1
1 1.000 0.080 14 104776883 non coding transcript exon variant G/A snv 0.33 0.700 1.000 1 2016 2016
dbSNP: rs2747716
rs2747716
LINC02523 ; LOC105377986
1 1.000 0.080 6 125687226 intron variant A/G;T snv 0.700 1.000 1 2018 2018
dbSNP: rs2797160
rs2797160
LINC02523 ; LOC105377986
1 1.000 0.080 6 125688970 intron variant A/G snv 0.48 0.700 1.000 1 2016 2016
dbSNP: rs35286446
rs35286446
LINC00824
1 1.000 0.080 8 128433618 intron variant TATATA/-;TATA;TATATATA;TATATATATA delins 0.700 1.000 1 2018 2018