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: rs10055201
rs10055201
IL31RA
3 0.882 0.080 5 55865274 intron variant A/G snv 0.76 0.010 1.000 1 2017 2017
dbSNP: rs10131293
rs10131293
LOC105370401
1 1.000 0.040 14 22461166 intron variant G/A snv 0.15 0.700 1.000 1 2009 2009
dbSNP: rs10132733
rs10132733
LOC105370401 ; LOC112267867
1 1.000 0.040 14 22477241 intron variant A/G snv 0.19 0.700 1.000 1 2009 2009
dbSNP: rs10142552
rs10142552
LOC105370401
1 1.000 0.040 14 22395232 intron variant G/A snv 3.5E-02 0.700 1.000 1 2009 2009
dbSNP: rs10148895
rs10148895 		1 1.000 0.040 14 22254840 intron variant C/T snv 0.18 0.700 1.000 1 2009 2009
dbSNP: rs10155916
rs10155916
LOC107986784
1 1.000 0.040 7 38286177 intergenic variant G/A snv 0.11 0.700 1.000 1 2009 2009
dbSNP: rs10162417
rs10162417
LOC105370401
1 1.000 0.040 14 22460708 intron variant T/G snv 0.15 0.700 1.000 1 2009 2009
dbSNP: rs1024611
rs1024611 		63 0.568 0.800 17 34252769 upstream gene variant A/G snv 0.28 0.010 1.000 1 2019 2019
dbSNP: rs1027702
rs1027702 		3 0.882 0.080 1 161743067 intergenic variant C/T snv 0.51 0.010 1.000 1 2017 2017
dbSNP: rs1039659576
rs1039659576
MTR
21 0.689 0.520 1 236803473 missense variant A/G snv 0.010 1.000 1 2014 2014
dbSNP: rs1040303
rs1040303
LOC105370401
1 1.000 0.040 14 22403377 intron variant G/A snv 0.13 0.700 1.000 1 2009 2009
dbSNP: rs1042522
rs1042522
TP53
242 0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 0.030 1.000 3 2017 2019
dbSNP: rs10441090
rs10441090 		1 1.000 0.040 7 38295217 upstream gene variant C/T snv 0.13 0.700 1.000 1 2009 2009
dbSNP: rs1045485
rs1045485
CASP8
34 0.637 0.480 2 201284866 missense variant G/A;C;T snv 4.0E-06; 9.0E-02 0.010 1.000 1 2014 2014
dbSNP: rs1047768
rs1047768
ERCC5 ; BIVM-ERCC5
20 0.695 0.320 13 102852167 synonymous variant T/C snv 0.52 0.59 0.010 1.000 1 2016 2016
dbSNP: rs1048108
rs1048108
BARD1 ; SNHG31
5 0.827 0.120 2 214809500 missense variant G/A snv 0.38 0.33 0.010 1.000 1 2018 2018
dbSNP: rs10483273
rs10483273
LOC105370401
1 1.000 0.040 14 22448054 intron variant A/G snv 9.5E-02 0.700 1.000 1 2009 2009
dbSNP: rs10483275
rs10483275
TRDC ; LOC105370401 ; LOC112267867
1 1.000 0.040 14 22464064 intron variant C/T snv 9.5E-02 0.700 1.000 1 2009 2009
dbSNP: rs10483277
rs10483277
LOC105370401 ; LOC112267867
1 1.000 0.040 14 22471852 intron variant C/G;T snv 0.700 1.000 1 2009 2009
dbSNP: rs10487742
rs10487742 		1 1.000 0.040 7 38326911 non coding transcript exon variant G/A snv 0.14 0.700 1.000 1 2009 2009
dbSNP: rs104893855
rs104893855
PHOX2B ; PHOX2B-AS1
4 0.851 0.160 4 41747479 missense variant C/A snv 0.010 1.000 1 2014 2014
dbSNP: rs104893856
rs104893856
PHOX2B
6 0.827 0.080 4 41746162 missense variant C/T snv 0.010 < 0.001 1 2006 2006
dbSNP: rs104893877
rs104893877
SNCA
59 0.614 0.360 4 89828149 missense variant C/T snv 0.050 1.000 5 2003 2018
dbSNP: rs104893878
rs104893878
SNCA ; SNCA-AS1
21 0.732 0.160 4 89835580 missense variant C/G snv 0.060 1.000 6 2003 2018
dbSNP: rs104893936
rs104893936
SNCB
4 0.851 0.120 5 176626472 missense variant C/G;T snv 5.6E-05 0.010 1.000 1 2007 2007