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: rs2292462
rs2292462
NMB
2 1.000 0.080 15 84657523 intron variant G/C;T snv 0.700 1.000 1 2018 2018
dbSNP: rs2361796
rs2361796
LILRB5
1 19 54250521 3 prime UTR variant T/G snv 0.27 0.700 1.000 1 2018 2018
dbSNP: rs2361797
rs2361797
LILRB5
1 19 54249685 3 prime UTR variant A/G snv 0.54 0.700 1.000 1 2014 2014
dbSNP: rs2693560
rs2693560 		1 6 117202508 intergenic variant A/G;T snv 0.700 1.000 1 2018 2018
dbSNP: rs2819598
rs2819598 		1 6 117132241 intergenic variant A/G;T snv 0.700 1.000 1 2018 2018
dbSNP: rs333947
rs333947
CSF1
7 1 109928142 intron variant G/A snv 0.13 0.700 1.000 1 2018 2018
dbSNP: rs3800963
rs3800963
SNX13
1 7 17940170 intron variant G/A snv 0.33 0.700 1.000 1 2018 2018
dbSNP: rs4665988
rs4665988
C2orf16
1 2 27538569 intron variant C/A;T snv 0.700 1.000 1 2018 2018
dbSNP: rs491626
rs491626
ABO
2 9 133269461 intron variant T/A;C snv 0.700 1.000 1 2018 2018
dbSNP: rs5763790
rs5763790
HORMAD2
1 22 30126424 intron variant G/C snv 0.75 0.700 1.000 1 2018 2018
dbSNP: rs61751507
rs61751507
CPN1
3 1.000 0.080 10 100069757 missense variant C/T snv 4.2E-02 3.4E-02 0.700 1.000 1 2018 2018
dbSNP: rs6501199
rs6501199 		1 17 78338705 intron variant G/C snv 0.60 0.700 1.000 1 2018 2018
dbSNP: rs6810325
rs6810325
CAND2
2 1.000 0.080 3 12799435 intron variant T/C snv 0.66 0.700 1.000 1 2018 2018
dbSNP: rs6871959
rs6871959 		1 5 158527363 intron variant G/A snv 0.36 0.700 1.000 1 2018 2018
dbSNP: rs7136716
rs7136716 		6 0.851 0.080 12 7538538 regulatory region variant A/G snv 0.22 0.700 1.000 1 2010 2010
dbSNP: rs7138813
rs7138813 		1 12 7580629 intergenic variant T/A;C;G snv 0.700 1.000 1 2018 2018
dbSNP: rs7147275
rs7147275
SAMD4A
1 14 54766806 intron variant G/A snv 0.16 0.700 1.000 1 2018 2018
dbSNP: rs7208815
rs7208815 		1 17 40012462 non coding transcript exon variant C/G;T snv 0.700 1.000 1 2018 2018
dbSNP: rs7487435
rs7487435 		1 12 7531072 intergenic variant C/A;T snv 0.700 1.000 1 2018 2018
dbSNP: rs76854597
rs76854597
ANO5
1 11 22200238 intron variant A/C;T snv 0.700 1.000 1 2018 2018
dbSNP: rs78139700
rs78139700
BVES ; BVES-AS1
1 6 105135997 intron variant C/G;T snv 8.2E-04 0.700 1.000 1 2018 2018
dbSNP: rs8101286
rs8101286
PEPD
1 19 33395807 intron variant T/A;G snv 0.700 1.000 1 2018 2018
dbSNP: rs9600129
rs9600129 		1 13 73531052 intron variant G/T snv 0.33 0.700 1.000 1 2018 2018
dbSNP: rs9607721
rs9607721
MRTFA
1 22 40466116 intron variant A/G snv 0.18 0.700 1.000 1 2018 2018
dbSNP: rs961183
rs961183
UBAP1
1 9 34243686 intron variant C/T snv 0.33 0.700 1.000 1 2018 2018