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: rs10863358
rs10863358
CR1
1 1 207517526 intron variant G/C snv 0.25 0.700 1.000 1 2012 2012
dbSNP: rs10888935
rs10888935
1 1 55595278 intron variant T/A snv 0.52 0.700 1.000 1 2012 2012
dbSNP: rs10908713
rs10908713
2 1 159369769 intron variant T/C snv 0.47 0.700 1.000 1 2012 2012
dbSNP: rs10908716
rs10908716
1 1 159406553 intron variant A/G snv 0.10 0.700 1.000 1 2012 2012
dbSNP: rs10908717
rs10908717
1 1 159406562 intron variant C/A snv 0.10 0.700 1.000 1 2012 2012
dbSNP: rs10908724
rs10908724
1 1 159480378 intron variant G/A;T snv 0.700 1.000 1 2012 2012
dbSNP: rs10908733
rs10908733
1 1 159534264 downstream gene variant T/A;C snv 0.700 1.000 1 2012 2012
dbSNP: rs11117956
rs11117956
CR1
1 1 207511014 intron variant T/G snv 0.26 0.700 1.000 1 2012 2012
dbSNP: rs11117959
rs11117959
CR1
1 1 207511174 intron variant A/G snv 0.19 0.700 1.000 1 2012 2012
dbSNP: rs11118131
rs11118131
CR1
1 1 207587851 intron variant C/T snv 0.20 0.700 1.000 1 2012 2012
dbSNP: rs11118135
rs11118135
CR1
1 1 207597083 intron variant A/G snv 0.20 0.700 1.000 1 2012 2012
dbSNP: rs11118136
rs11118136
CR1
1 1 207599063 intron variant A/G snv 0.20 0.700 1.000 1 2012 2012
dbSNP: rs11118157
rs11118157
CR1
1 1 207604974 intron variant C/A snv 0.41 0.700 1.000 1 2012 2012
dbSNP: rs11118166
rs11118166
CR1
1 1 207608650 intron variant A/G snv 0.38 0.700 1.000 1 2012 2012
dbSNP: rs11118167
rs11118167
CR1
1 1 207608809 intron variant T/C snv 0.15 0.700 1.000 1 2012 2012
dbSNP: rs11265142
rs11265142
1 1 159130118 intron variant A/G snv 8.4E-02 0.700 1.000 1 2012 2012
dbSNP: rs11265174
rs11265174
2 1 159350569 intron variant T/A snv 0.35 0.700 1.000 1 2012 2012
dbSNP: rs11265177
rs11265177
1 1 159356044 intron variant A/G snv 0.16 0.700 1.000 1 2012 2012
dbSNP: rs11265180
rs11265180
1 1 159373858 intron variant G/C snv 0.11 0.700 1.000 1 2012 2012
dbSNP: rs11265186
rs11265186
1 1 159406113 non coding transcript exon variant C/T snv 0.11 0.700 1.000 1 2012 2012
dbSNP: rs11265187
rs11265187
1 1 159408804 intron variant C/A;T snv 0.700 1.000 1 2012 2012
dbSNP: rs11265190
rs11265190
2 1 159421611 intron variant G/A snv 0.47 0.700 1.000 1 2012 2012
dbSNP: rs11265191
rs11265191
2 1 159430569 intron variant C/G;T snv 0.700 1.000 1 2012 2012
dbSNP: rs11265193
rs11265193
1 1 159431866 intron variant G/T snv 0.11 0.700 1.000 1 2012 2012
dbSNP: rs11265194
rs11265194
1 1 159433899 intron variant G/T snv 0.63 0.700 1.000 1 2012 2012