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: rs11165643
rs11165643 		2 1 96458541 intergenic variant C/T snv 0.48 0.700 1.000 6 2015 2019
dbSNP: rs1167827
rs1167827
HIP1
5 7 75533848 3 prime UTR variant G/A snv 0.37 0.700 1.000 6 2015 2018
dbSNP: rs12885454
rs12885454
LOC102724934
4 14 29267632 non coding transcript exon variant C/A snv 0.27 0.700 1.000 6 2015 2019
dbSNP: rs13191362
rs13191362
PRKN
3 6 162612318 intron variant A/G snv 8.7E-02 0.700 1.000 6 2015 2019
dbSNP: rs16851483
rs16851483
RASA2
4 0.925 0.080 3 141556594 intron variant G/T snv 6.7E-02 0.700 1.000 6 2015 2019
dbSNP: rs16907751
rs16907751 		1 8 80463222 intron variant C/T snv 0.10 0.700 1.000 6 2015 2019
dbSNP: rs2033529
rs2033529
TDRG1
4 6 40380914 intron variant A/C;G snv 0.700 1.000 6 2015 2019
dbSNP: rs2228213
rs2228213
HIVEP1
1 6 12124622 missense variant G/A snv 0.30 0.26 0.700 1.000 6 2015 2019
dbSNP: rs29941
rs29941 		6 1.000 0.080 19 33818627 downstream gene variant A/G snv 0.70 0.700 1.000 6 2009 2018
dbSNP: rs7124681
rs7124681
CELF1
2 11 47508395 intron variant C/A snv 0.36 0.700 1.000 6 2015 2019
dbSNP: rs7141420
rs7141420
NRXN3
5 1.000 0.080 14 79433111 intron variant C/T snv 0.56 0.700 1.000 6 2015 2019
dbSNP: rs7599312
rs7599312
LOC107985979
3 2 212548507 regulatory region variant G/A snv 0.29 0.700 1.000 6 2015 2019
dbSNP: rs9939609
rs9939609
FTO
98 0.559 0.720 16 53786615 intron variant T/A snv 0.41 0.700 1.000 6 2007 2019
dbSNP: rs10920678
rs10920678
BRINP3
1 1 190270777 intron variant A/G snv 0.58 0.700 1.000 5 2015 2019
dbSNP: rs10968576
rs10968576
LINGO2
10 0.882 0.120 9 28414341 intron variant A/G snv 0.26 0.700 1.000 5 2010 2018
dbSNP: rs12286929
rs12286929 		4 0.925 0.080 11 115151684 intergenic variant A/C;G snv 0.700 1.000 5 2015 2019
dbSNP: rs12454712
rs12454712
BCL2
9 0.925 0.120 18 63178651 intron variant T/A;C snv 0.700 1.000 5 2016 2019
dbSNP: rs13130484
rs13130484 		7 1.000 0.080 4 45173674 intergenic variant C/A;T snv 0.700 1.000 5 2013 2019
dbSNP: rs17094222
rs17094222 		3 0.925 0.080 10 100635683 intergenic variant T/C snv 0.17 0.700 1.000 5 2015 2019
dbSNP: rs17724992
rs17724992
PGPEP1
1 19 18344015 intron variant A/G snv 0.23 0.700 1.000 5 2015 2018
dbSNP: rs205262
rs205262
ILRUN
2 6 34595387 intron variant A/G snv 0.38 0.700 1.000 5 2015 2018
dbSNP: rs2075650
rs2075650
TOMM40
45 0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13 0.700 1.000 5 2015 2019
dbSNP: rs2245368
rs2245368
DTX2P1-UPK3BP1-PMS2P11 ; LOC105375361
3 7 76978826 non coding transcript exon variant C/T snv 0.80 0.700 1.000 5 2015 2018
dbSNP: rs2287019
rs2287019
QPCTL
7 1.000 0.080 19 45698914 intron variant C/T snv 0.17 0.16 0.700 1.000 5 2010 2018
dbSNP: rs2531995
rs2531995
ADCY9
7 1.000 0.080 16 3963466 3 prime UTR variant C/T snv 0.45 0.700 1.000 5 2014 2019