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: rs3181238
rs3181238
TDP2
1 6 24654215 intron variant C/G;T snv 0.700 1.000 1 2018 2018
dbSNP: rs381254
rs381254
MAMSTR
1 19 48717947 intron variant C/T snv 0.92 0.700 1.000 1 2018 2018
dbSNP: rs4654971
rs4654971
ALPL
1 1 21571410 intron variant T/C snv 7.8E-02 0.700 1.000 1 2019 2019
dbSNP: rs4962153
rs4962153
ADAMTS13 ; CACFD1
9 0.925 0.120 9 133458632 intron variant A/G snv 0.79 0.700 1.000 1 2008 2008
dbSNP: rs505922
rs505922
ABO
34 0.689 0.520 9 133273813 intron variant C/T snv 0.700 1.000 1 2017 2017
dbSNP: rs58270597
rs58270597
TRIM5
1 11 5667453 intron variant C/T snv 0.14 0.700 1.000 1 2018 2018
dbSNP: rs6911965
rs6911965
GPLD1
2 6 24480067 intron variant T/A;C snv 0.700 1.000 1 2010 2010
dbSNP: rs6984305
rs6984305 		1 8 9320758 intron variant A/T snv 0.85 0.800 1.000 1 2011 2011
dbSNP: rs71357834
rs71357834
FAM83E
1 19 48604360 intron variant C/T snv 9.4E-02 0.700 1.000 1 2018 2018
dbSNP: rs7267979
rs7267979
ABHD12
1 20 25317451 intron variant A/G snv 0.58 0.800 1.000 1 2011 2011
dbSNP: rs74612335
rs74612335
ST3GAL4
1 11 126368738 intron variant T/C snv 0.15 0.700 1.000 1 2018 2018
dbSNP: rs74614333
rs74614333
ALPL
1 1 21518031 intron variant T/A snv 0.13 0.700 1.000 1 2018 2018
dbSNP: rs77972946
rs77972946
RAP1GAP
1 1 21628472 intron variant C/A;G;T snv 0.700 1.000 1 2018 2018
dbSNP: rs78406497
rs78406497
DENND2B ; LOC102724784
1 11 8804524 intron variant G/A snv 5.1E-02 0.700 1.000 1 2018 2018
dbSNP: rs7923609
rs7923609
JMJD1C ; MIR1296
1 10 63374062 intron variant A/G snv 0.43 0.800 1.000 1 2011 2011
dbSNP: rs79343853
rs79343853
ABO
1 9 133270880 intron variant T/C snv 0.700 1.000 1 2018 2018
dbSNP: rs7966590
rs7966590
B4GALNT3
1 12 461674 intron variant G/A;C snv 0.700 1.000 1 2018 2018
dbSNP: rs9467160
rs9467160
GPLD1
3 6 24441518 intron variant G/A snv 0.29 0.700 1.000 1 2008 2008
dbSNP: rs9467191
rs9467191
GPLD1
1 6 24475554 intron variant C/A snv 0.15 0.700 1.000 1 2018 2018
dbSNP: rs9533090
rs9533090
LINC02341
3 13 42377313 intron variant C/T snv 0.39 0.700 1.000 1 2018 2018
dbSNP: rs10819937
rs10819937 		1 9 101460951 intergenic variant C/G;T snv 0.800 1.000 1 2011 2011
dbSNP: rs1780324
rs1780324 		3 1 21495264 intergenic variant A/G snv 0.48 0.700 1.000 1 2008 2008
dbSNP: rs73766540
rs73766540 		1 5 82427213 intergenic variant T/A;C snv 0.700 1.000 1 2018 2018
dbSNP: rs9533177
rs9533177 		1 13 42615089 intergenic variant G/T snv 0.40 0.700 1.000 1 2018 2018
dbSNP: rs2183745
rs2183745
LOC105376184
1 9 101456893 regulatory region variant T/A snv 0.65 0.700 1.000 1 2018 2018