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: rs10737680
rs10737680
CFH
9 0.827 0.080 1 196710325 intron variant A/C snv 0.44 0.700 1.000 1 2015 2015
dbSNP: rs10746379
rs10746379
TGFB2
1 1 218402545 intron variant A/G snv 0.20 0.700 1.000 1 2015 2015
dbSNP: rs1075472
rs1075472
RIN3
1 14 92641786 intron variant A/G;T snv 0.700 1.000 1 2015 2015
dbSNP: rs10801558
rs10801558
CFH
2 1.000 0.040 1 196729914 intron variant T/G snv 0.46 0.700 1.000 1 2015 2015
dbSNP: rs10801559
rs10801559
CFH
2 1.000 0.040 1 196735074 intron variant G/A snv 0.44 0.700 1.000 1 2015 2015
dbSNP: rs10851907
rs10851907
CHRNB4
4 1.000 0.040 15 78623522 upstream gene variant G/A snv 0.40 0.700 1.000 1 2015 2015
dbSNP: rs10863398
rs10863398
TGFB2
2 1 218414937 intron variant G/A;C snv 0.700 1.000 1 2015 2015
dbSNP: rs10922104
rs10922104
CFH
2 1.000 0.040 1 196718600 intron variant A/C;G snv 0.700 1.000 1 2015 2015
dbSNP: rs10922105
rs10922105
CFH
2 1.000 0.040 1 196721120 intron variant A/C;T snv 0.700 1.000 1 2015 2015
dbSNP: rs10922106
rs10922106
CFH
4 0.925 0.080 1 196722334 intron variant A/G snv 0.43 0.700 1.000 1 2015 2015
dbSNP: rs10922108
rs10922108
CFH
2 1.000 0.040 1 196732343 intron variant A/T snv 0.46 0.700 1.000 1 2015 2015
dbSNP: rs10922109
rs10922109
CFH
6 0.827 0.080 1 196735502 intron variant C/A snv 0.46 0.700 1.000 1 2015 2015
dbSNP: rs11072785
rs11072785
CHRNB4 ; LOC112268142
3 15 78675887 intron variant C/T snv 0.28 0.700 1.000 1 2015 2015
dbSNP: rs11072790
rs11072790
CHRNB4 ; LOC105370913 ; LOC112268142
2 15 78699683 intron variant C/T snv 0.31 0.700 1.000 1 2015 2015
dbSNP: rs11072791
rs11072791
CHRNB4 ; LOC105370913 ; LOC112268142
3 15 78704734 intron variant C/A snv 0.29 0.700 1.000 1 2015 2015
dbSNP: rs11072792
rs11072792
CHRNB4 ; LOC105370913 ; LOC112268142
2 15 78707569 intron variant A/G snv 0.30 0.700 1.000 1 2015 2015
dbSNP: rs11072803
rs11072803
ADAMTS7
1 15 78785536 intron variant G/A snv 0.34 0.700 1.000 1 2015 2015
dbSNP: rs11072804
rs11072804
ADAMTS7
1 15 78786144 intron variant T/G snv 0.700 1.000 1 2015 2015
dbSNP: rs11072805
rs11072805
ADAMTS7
1 15 78786176 intron variant T/C snv 0.700 1.000 1 2015 2015
dbSNP: rs11072806
rs11072806
ADAMTS7
1 15 78786732 intron variant G/A snv 0.32 0.700 1.000 1 2015 2015
dbSNP: rs1108581
rs1108581
DBH
3 1.000 0.080 9 133640119 intron variant A/G snv 0.27 0.700 1.000 1 2015 2015
dbSNP: rs11100860
rs11100860
LOC105377462
4 4 144557987 intron variant A/G snv 0.43 0.700 1.000 1 2015 2015
dbSNP: rs11118112
rs11118112
LINC02869
1 1 218499915 intron variant C/T snv 0.16 0.700 1.000 1 2015 2015
dbSNP: rs11118114
rs11118114
LINC02869
1 1 218506344 intron variant G/A snv 0.16 0.700 1.000 1 2015 2015
dbSNP: rs11118118
rs11118118
LINC02869
1 1 218520349 intron variant T/G snv 0.16 0.700 1.000 1 2015 2015