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: rs10852151
rs10852151 		1 1.000 0.040 15 91540065 intron variant A/G;T snv 0.700 1.000 1 2017 2017
dbSNP: rs12465911
rs12465911 		2 0.925 0.080 2 150929228 intergenic variant C/T snv 0.21 0.700 1.000 1 2018 2018
dbSNP: rs12792379
rs12792379 		1 1.000 0.040 11 6247316 downstream gene variant G/A snv 0.21 0.700 1.000 1 2019 2019
dbSNP: rs1297211
rs1297211 		1 1.000 0.040 21 14956635 intron variant C/G snv 0.47 0.700 1.000 1 2019 2019
dbSNP: rs13396805
rs13396805 		2 0.925 0.080 2 150964998 intergenic variant C/T snv 0.20 0.010 1.000 1 2018 2018
dbSNP: rs1363119
rs1363119 		2 1.000 0.040 19 18333999 downstream gene variant A/G;T snv 0.700 1.000 1 2019 2019
dbSNP: rs2341926
rs2341926 		2 0.925 0.080 2 150927414 intergenic variant A/G snv 0.20 0.010 1.000 1 2018 2018
dbSNP: rs4676893
rs4676893 		3 0.882 0.080 3 70868488 intergenic variant A/T snv 0.61 0.700 1.000 1 2019 2019
dbSNP: rs72771256
rs72771256 		1 1.000 0.040 5 83588743 intergenic variant G/A;T snv 0.700 1.000 1 2019 2019
dbSNP: rs7613875
rs7613875 		2 1.000 0.040 3 49934081 upstream gene variant C/A;G;T snv 0.700 1.000 1 2019 2019
dbSNP: rs9936833
rs9936833 		6 0.882 0.160 16 86369512 intergenic variant C/T snv 0.64 0.010 1.000 1 2017 2017
dbSNP: rs4965272
rs4965272
ADAMTS17
1 1.000 0.040 15 100044534 intron variant T/A;G snv 0.35 0.010 1.000 1 2019 2019
dbSNP: rs7609078
rs7609078
AFF3
1 1.000 0.040 2 99873901 intron variant G/A snv 0.37 0.700 1.000 1 2019 2019
dbSNP: rs11901649
rs11901649
APOB
3 0.882 0.080 2 21027351 intron variant G/A;C;T snv 0.700 1.000 1 2019 2019
dbSNP: rs597808
rs597808
ATXN2
19 0.742 0.200 12 111535554 intron variant A/G snv 0.67 0.700 1.000 1 2019 2019
dbSNP: rs11789015
rs11789015
BARX1
6 0.882 0.080 9 93953746 intron variant A/C;G snv 0.010 1.000 1 2019 2019
dbSNP: rs7763910
rs7763910
BTN2A1 ; LOC285819
1 1.000 0.040 6 26472427 intron variant A/G snv 0.48 0.700 1.000 1 2019 2019
dbSNP: rs7282609
rs7282609
C21orf62-AS1 ; LOC105377136
1 1.000 0.040 21 32906849 intron variant A/G snv 0.34 0.700 1.000 1 2019 2019
dbSNP: rs7552188
rs7552188
DPYD
1 1.000 0.040 1 97838601 intron variant T/C snv 0.74 0.700 1.000 1 2019 2019
dbSNP: rs7644468
rs7644468
EPHA6
1 1.000 0.040 3 97291143 intron variant T/C snv 1.4E-02 0.010 1.000 1 2011 2011
dbSNP: rs759412116
rs759412116
ERCC2
55 0.581 0.640 19 45352210 missense variant C/G;T snv 4.0E-06; 6.0E-05 0.010 1.000 1 2005 2005
dbSNP: rs13181
rs13181
ERCC2 ; KLC3
134 0.487 0.760 19 45351661 stop gained T/A;G snv 4.0E-06; 0.32 0.010 1.000 1 2005 2005
dbSNP: rs10228350
rs10228350
FOXP2
2 1.000 0.040 7 114420608 intron variant A/G;T snv 0.700 1.000 1 2019 2019
dbSNP: rs5443
rs5443
GNB3 ; CDCA3
106 0.532 0.760 12 6845711 synonymous variant C/T snv 0.36 0.44 0.010 1.000 1 2009 2009
dbSNP: rs12706746
rs12706746
GRM8
1 1.000 0.040 7 126802805 intron variant G/A snv 0.24 0.700 1.000 1 2019 2019