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: rs1001989
rs1001989 		1 8 106844987 intergenic variant T/C;G snv 0.700 1.000 1 2018 2018
dbSNP: rs10036789
rs10036789 		3 1.000 0.080 5 72400091 regulatory region variant C/A;G snv 0.700 1.000 3 2018 2018
dbSNP: rs10071507
rs10071507
ADAMTS6
1 5 65342512 intron variant T/C snv 0.27 0.700 1.000 1 2018 2018
dbSNP: rs10105844
rs10105844
ANGPT1
1 8 107278644 intron variant G/A snv 0.78 0.700 1.000 1 2017 2017
dbSNP: rs10127863
rs10127863
GTF2B
1 1 88878573 intron variant G/A snv 0.48 0.700 1.000 1 2018 2018
dbSNP: rs10140566
rs10140566
DPF3
1 14 72665482 intron variant T/A;G snv 0.700 1.000 1 2018 2018
dbSNP: rs10172196
rs10172196
FEZ2
1 2 36553406 intron variant G/A snv 0.26 0.700 1.000 1 2018 2018
dbSNP: rs10173269
rs10173269
ANTXR1
1 2 69180588 intron variant T/G snv 0.57 0.700 1.000 1 2018 2018
dbSNP: rs10180371
rs10180371
PARD3B
1 2 205150255 intron variant A/G snv 0.64 0.700 1.000 1 2018 2018
dbSNP: rs10189434
rs10189434
BABAM2
1 2 28135884 intron variant C/T snv 0.23 0.700 1.000 2 2018 2018
dbSNP: rs10230941
rs10230941 		1 7 117996057 downstream gene variant C/G;T snv 0.700 1.000 2 2018 2018
dbSNP: rs10233003
rs10233003
CAV2
1 7 116503608 intron variant C/A snv 0.27 0.700 1.000 1 2018 2018
dbSNP: rs10258482
rs10258482 		1 7 116510041 downstream gene variant C/A snv 0.28 0.700 1.000 2 2014 2017
dbSNP: rs10281637
rs10281637 		2 1.000 0.040 7 116511284 downstream gene variant T/C snv 0.28 0.700 1.000 3 2017 2018
dbSNP: rs1035673
rs1035673
TNS1
1 2 217810810 intron variant T/C snv 0.65 0.700 1.000 1 2017 2017
dbSNP: rs1042499
rs1042499
ANPEP
1 15 89785074 3 prime UTR variant T/C snv 5.2E-02 0.700 1.000 1 2018 2018
dbSNP: rs1042602
rs1042602
TYR ; LOC107984363
6 0.925 0.080 11 89178528 missense variant C/A snv 0.25 0.24 0.700 1.000 1 2018 2018
dbSNP: rs10447301
rs10447301
ADAMTS2
1 5 179122253 intron variant G/A;C snv 0.700 1.000 1 2018 2018
dbSNP: rs1044864
rs1044864
ANAPC1
2 2 111769289 3 prime UTR variant G/A snv 0.20 0.18 0.700 1.000 1 2018 2018
dbSNP: rs1047922
rs1047922
ZNF516
1 18 76358607 splice region variant T/C snv 0.12 0.700 1.000 2 2018 2018
dbSNP: rs10502235
rs10502235
ARHGEF12
1 11 120341714 intron variant A/G snv 0.19 0.700 1.000 1 2015 2015
dbSNP: rs10505102
rs10505102
ANGPT1
1 8 107276121 intron variant T/A snv 0.13 0.700 1.000 1 2018 2018
dbSNP: rs10507170
rs10507170
TTC41P
1 12 103851268 intron variant G/A snv 9.2E-02 0.700 1.000 1 2018 2018
dbSNP: rs10508700
rs10508700
GPR158
1 10 25532389 intron variant T/C snv 0.60 0.700 1.000 1 2018 2018
dbSNP: rs10563220
rs10563220 		1 7 65857401 downstream gene variant TATATATATA/-;TA;TATA;TATATA;TATATATA;TATATATATATA;TATATATATATATA;TATATATATATATATA;TATATATATATATATATA;TATATATATATATATATATA;TATATATATATATATATATATA;TATATATATATATATATATATATA delins 0.700 1.000 1 2019 2019