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: rs10894604
rs10894604
OPCML
1 11 132771851 non coding transcript exon variant T/G snv 0.26 0.800 1.000 1 2013 2013
dbSNP: rs17213965
rs17213965
MYH11
1 16 15788110 intron variant C/T snv 0.24 0.800 1.000 1 2013 2013
dbSNP: rs2074356
rs2074356
HECTD4
18 0.763 0.280 12 112207597 intron variant G/A snv 3.8E-03 0.800 1.000 1 2009 2009
dbSNP: rs2076529
rs2076529
BTNL2 ; TSBP1-AS1
2 1.000 0.120 6 32396178 synonymous variant T/C snv 0.41 0.39 0.800 1.000 1 2010 2010
dbSNP: rs2820464
rs2820464
LYPLAL1-AS1
1 1 219519878 intergenic variant G/A;C snv 0.800 1.000 1 2013 2013
dbSNP: rs4846567
rs4846567 		1 1 219577375 regulatory region variant G/T snv 0.23 0.800 1.000 1 2010 2010
dbSNP: rs6784615
rs6784615
NISCH
2 1.000 0.080 3 52472410 intron variant C/T snv 0.96 0.96 0.800 1.000 1 2010 2010
dbSNP: rs6795735
rs6795735
ADAMTS9-AS2
7 0.882 0.120 3 64719689 intron variant C/A;G;T snv 0.800 1.000 1 2010 2010
dbSNP: rs6931262
rs6931262
RREB1
1 6 7217284 non coding transcript exon variant C/T snv 0.10 0.800 1.000 1 2013 2013
dbSNP: rs7745274
rs7745274
RSPO3 ; LOC112267972
1 6 127188012 intron variant G/A snv 0.56 0.800 1.000 1 2013 2013
dbSNP: rs10019888
rs10019888 		3 4 26061368 regulatory region variant A/G snv 0.17 0.700 1.000 1 2019 2019
dbSNP: rs10024899
rs10024899 		1 4 121705035 intergenic variant T/C snv 0.35 0.700 1.000 1 2019 2019
dbSNP: rs10049088
rs10049088
LINC02029
3 3 157079859 upstream gene variant C/T snv 0.35 0.700 1.000 1 2019 2019
dbSNP: rs1006195
rs1006195
HMBS
1 11 119088159 non coding transcript exon variant G/T snv 0.33 0.700 1.000 1 2019 2019
dbSNP: rs10065321
rs10065321
SPRY4-AS1
1 5 142477850 intron variant C/T snv 0.38 0.700 1.000 1 2019 2019
dbSNP: rs1006705
rs1006705
FLJ12825
1 12 54065146 intron variant A/G snv 0.66 0.700 1.000 1 2019 2019
dbSNP: rs10070064
rs10070064 		1 5 173854774 intergenic variant C/T snv 0.26 0.700 1.000 1 2019 2019
dbSNP: rs1007330
rs1007330
EYA2
1 20 46897482 intron variant C/T snv 0.33 0.700 1.000 1 2019 2019
dbSNP: rs10083447
rs10083447
TRIP11
1 14 91998083 intron variant G/A snv 0.52 0.700 1.000 1 2019 2019
dbSNP: rs10101067
rs10101067
EYA1
2 8 71495139 intron variant G/C snv 6.2E-02 0.700 1.000 1 2019 2019
dbSNP: rs10116353
rs10116353
EPB41L4B
1 9 109187808 intron variant G/T snv 0.32 0.700 1.000 1 2019 2019
dbSNP: rs10125521
rs10125521
LINC01505
1 9 106300721 intron variant G/A;C;T snv 0.700 1.000 1 2019 2019
dbSNP: rs10132280
rs10132280 		6 14 25458973 intergenic variant C/A snv 0.37 0.700 1.000 1 2019 2019
dbSNP: rs10152595
rs10152595
SMAD3
2 1.000 0.080 15 67183150 intron variant C/G;T snv 0.700 1.000 1 2019 2019
dbSNP: rs10153926
rs10153926
LOC112268413
1 2 42961980 intergenic variant G/A snv 0.21 0.700 1.000 1 2019 2019