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: rs10913200
rs10913200
PAPPA2
1 1 176552519 intron variant G/A snv 1.8E-02 0.700 1.000 1 2019 2019
dbSNP: rs10985827
rs10985827
RABGAP1
1 9 122939329 non coding transcript exon variant T/G snv 0.34 0.700 1.000 1 2019 2019
dbSNP: rs1101081
rs1101081
ESR1
1 6 151711782 intron variant C/T snv 0.26 0.700 1.000 1 2016 2016
dbSNP: rs11042596
rs11042596 		1 11 2097630 intergenic variant T/G snv 0.73 0.700 1.000 1 2019 2019
dbSNP: rs11051061
rs11051061
LOC645485 ; LINC00941
1 12 30761734 intron variant G/A snv 0.19 0.700 1.000 1 2019 2019
dbSNP: rs11055030
rs11055030
APOLD1 ; LOC105369663 ; LOC107984129
1 12 12725415 upstream gene variant G/C snv 0.23 0.700 1.000 1 2019 2019
dbSNP: rs11055034
rs11055034
APOLD1 ; LOC107984129
2 1.000 0.080 12 12737692 intron variant C/A;T snv 0.700 1.000 1 2016 2016
dbSNP: rs11082304
rs11082304
CABLES1
6 18 23141009 intron variant G/C;T snv 0.700 1.000 1 2019 2019
dbSNP: rs11085720
rs11085720
DNMT1
1 19 10207087 intron variant A/G snv 0.54 0.700 1.000 1 2019 2019
dbSNP: rs1112718
rs1112718 		1 10 92719350 intergenic variant A/G snv 0.43 0.700 1.000 1 2019 2019
dbSNP: rs112139215
rs112139215
MLXIPL
1 7 73620229 intron variant C/A snv 4.1E-02 0.700 1.000 1 2019 2019
dbSNP: rs1129156
rs1129156
MAP3K10
1 19 40213169 synonymous variant T/C snv 0.73 0.75 0.700 1.000 1 2019 2019
dbSNP: rs113086489
rs113086489 		1 17 7268037 upstream gene variant C/A;G;T snv 0.700 1.000 1 2016 2016
dbSNP: rs113510833
rs113510833 		1 6 29703290 downstream gene variant C/T snv 6.7E-02 0.700 1.000 1 2019 2019
dbSNP: rs1151200
rs1151200
TENM4
2 11 79281641 intron variant T/C snv 0.50 0.700 1.000 1 2012 2012
dbSNP: rs11545169
rs11545169
PSMD2
3 3 184302754 missense variant G/T snv 0.13 0.11 0.700 1.000 1 2019 2019
dbSNP: rs116276359
rs116276359
THEM5 ; C2CD4D-AS1
1 1 151848954 intron variant C/A snv 1.5E-02 0.700 1.000 1 2019 2019
dbSNP: rs11630479
rs11630479
IGF1R
1 15 98697252 intron variant G/A snv 0.39 0.700 1.000 1 2019 2019
dbSNP: rs11641308
rs11641308 		1 16 75278125 intergenic variant T/C snv 0.52 0.700 1.000 1 2019 2019
dbSNP: rs11646700
rs11646700
SMPD3
1 16 68387765 intron variant A/G snv 0.38 0.700 1.000 1 2019 2019
dbSNP: rs116807401
rs116807401
PABPC4L
1 4 134200566 missense variant T/C snv 8.8E-03 9.5E-03 0.700 1.000 1 2019 2019
dbSNP: rs11680809
rs11680809 		1 2 112813232 downstream gene variant C/A snv 0.55 0.700 1.000 1 2019 2019
dbSNP: rs116964396
rs116964396
NKX6-3
1 8 41648330 intron variant C/A;T snv 0.700 1.000 1 2019 2019
dbSNP: rs11698914
rs11698914
COMMD7
1 20 32739337 intron variant C/A;G snv 0.700 1.000 1 2019 2019
dbSNP: rs11704481
rs11704481
FAM118A
1 22 45336447 intron variant G/A snv 0.49 0.42 0.700 1.000 1 2019 2019