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: rs10510181
rs10510181
CHL1-AS2
4 0.882 0.200 3 149364 intron variant G/A snv 0.31 0.700 1.000 1 2011 2011
dbSNP: rs11190870
rs11190870 		6 0.827 0.200 10 101219450 intergenic variant T/A;C snv 0.700 1.000 1 2013 2013
dbSNP: rs11598564
rs11598564 		3 0.925 0.200 10 101204847 intergenic variant G/A snv 0.45 0.700 1.000 1 2013 2013
dbSNP: rs12946942
rs12946942 		4 0.882 0.200 17 71240857 intergenic variant G/T snv 7.5E-02 0.700 1.000 1 2013 2013
dbSNP: rs147296805
rs147296805
MAPK7
1 17 19381095 missense variant G/A;T snv 5.0E-04; 8.0E-06 0.700 1.000 1 2017 2017
dbSNP: rs1555613564
rs1555613564
MAPK7
1 17 19382246 missense variant C/T snv 0.700 1.000 1 2017 2017
dbSNP: rs1828853
rs1828853
MIR4300HG
3 0.925 0.040 11 82371520 intron variant G/A;C;T snv 0.700 1.000 1 2017 2017
dbSNP: rs625039
rs625039
LBX1-AS1
3 0.925 0.200 10 101233892 intron variant G/A snv 0.22 0.700 1.000 1 2013 2013
dbSNP: rs6570507
rs6570507
ADGRG6
13 0.827 0.240 6 142358435 intron variant G/A snv 0.47 0.700 1.000 1 2013 2013
dbSNP: rs758163506
rs758163506
MAPK7
1 17 19382063 missense variant C/T snv 9.9E-06 7.0E-06 0.700 1.000 1 2017 2017
dbSNP: rs9496346
rs9496346
ADGRG6
4 1.000 0.040 6 142348201 intron variant A/G snv 0.42 0.700 1.000 1 2013 2013