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: rs10815094
rs10815094
RCL1
2 9 4845520 intron variant A/C;G snv 0.700 1.000 1 2009 2009
dbSNP: rs10815095
rs10815095
RCL1 ; MIR101-2
4 9 4848297 intron variant A/G snv 0.19 0.700 1.000 1 2009 2009
dbSNP: rs10815098
rs10815098
RCL1
2 9 4865338 intron variant C/T snv 0.24 0.700 1.000 1 2009 2009
dbSNP: rs10872428
rs10872428 		2 6 135170734 intergenic variant G/T snv 0.20 0.700 1.000 1 2009 2009
dbSNP: rs10900218
rs10900218
MARCHF8 ; LOC105378286
2 10 45465974 intron variant A/C;G snv 0.700 1.000 1 2009 2009
dbSNP: rs10946800
rs10946800 		4 0.925 0.120 6 25957545 intergenic variant C/T snv 0.37 0.700 1.000 1 2009 2009
dbSNP: rs10953302
rs10953302
ZAN
1 7 100767944 synonymous variant C/T snv 0.23 0.20 0.700 1.000 1 2009 2009
dbSNP: rs10974772
rs10974772 		1 9 4767677 downstream gene variant C/T snv 0.21 0.700 1.000 1 2009 2009
dbSNP: rs10974808
rs10974808
RCL1
3 9 4840380 intron variant A/G snv 9.0E-02 0.700 1.000 1 2009 2009
dbSNP: rs10974815
rs10974815
RCL1
2 9 4854253 intron variant C/T snv 0.11 0.700 1.000 1 2009 2009
dbSNP: rs11066188
rs11066188
HECTD4
7 0.851 0.320 12 112172910 intron variant G/A;C snv 0.30; 4.1E-06 0.700 1.000 1 2009 2009
dbSNP: rs11066301
rs11066301
PTPN11
12 0.827 0.200 12 112433568 intron variant A/G snv 0.30 0.700 1.000 1 2009 2009
dbSNP: rs11066320
rs11066320
PTPN11
5 0.925 0.120 12 112468611 intron variant A/G snv 0.70 0.700 1.000 1 2009 2009
dbSNP: rs11085822
rs11085822
DNASE2 ; MAST1
2 19 12874762 synonymous variant A/G snv 0.34 0.34 0.700 1.000 1 2009 2009
dbSNP: rs11085825
rs11085825
GCDH
3 19 12896644 intron variant C/T snv 0.31 0.700 1.000 1 2009 2009
dbSNP: rs11089823
rs11089823 		4 22 37113139 upstream gene variant T/C snv 0.28 0.700 1.000 1 2009 2009
dbSNP: rs11089824
rs11089824 		4 22 37113146 upstream gene variant A/C;T snv 0.700 1.000 1 2009 2009
dbSNP: rs11154794
rs11154794
MYB
2 6 135194310 intron variant T/C snv 0.12 0.15 0.700 1.000 1 2009 2009
dbSNP: rs11185506
rs11185506
TFRC
2 3 196070705 intron variant G/A;C snv 0.700 1.000 1 2009 2009
dbSNP: rs1130000
rs1130000
TRIM38
4 0.925 0.120 6 25985168 3 prime UTR variant A/G snv 0.37 0.700 1.000 1 2009 2009
dbSNP: rs1150660
rs1150660 		5 0.925 0.120 6 26101212 upstream gene variant A/C snv 0.73 0.700 1.000 1 2009 2009
dbSNP: rs115810
rs115810
TRIM38
5 0.925 0.120 6 25975655 intron variant G/A;C snv 0.700 1.000 1 2009 2009
dbSNP: rs11627531
rs11627531
FNTB ; MAX ; CHURC1-FNTB
2 14 65021078 intron variant T/C snv 0.57 0.700 1.000 1 2009 2009
dbSNP: rs11671604
rs11671604
HOOK2
2 19 12820875 intron variant A/T snv 0.20 0.700 1.000 1 2009 2009
dbSNP: rs11753329
rs11753329
USP49
2 6 41820642 intron variant T/G snv 0.14 0.700 1.000 1 2009 2009