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: rs603089
rs603089
2 0.925 0.120 6 25877742 intron variant G/A snv 0.36 0.700 1.000 3 2010 2013
dbSNP: rs1165168
rs1165168
2 0.925 0.120 6 25859280 intron variant A/C snv 0.16 0.700 1.000 2 2010 2013
dbSNP: rs1165206
rs1165206
2 0.925 0.120 6 25867338 intron variant G/A snv 0.55 0.700 1.000 2 2010 2013
dbSNP: rs1177441
rs1177441
2 0.925 0.120 6 25859185 intron variant A/G snv 0.16 0.700 1.000 2 2010 2013
dbSNP: rs1324087
rs1324087
2 0.925 0.120 6 25841180 intron variant G/A snv 0.15 0.700 1.000 2 2010 2013
dbSNP: rs1324088
rs1324088
2 0.925 0.120 6 25840894 intron variant G/A;T snv 0.700 1.000 2 2010 2013
dbSNP: rs523383
rs523383
2 0.925 0.120 6 25869620 intron variant A/G snv 0.20 0.700 1.000 2 2010 2013
dbSNP: rs555460
rs555460
2 0.925 0.120 6 25870427 intron variant C/T snv 0.20 0.700 1.000 2 2010 2013
dbSNP: rs972087
rs972087
2 0.925 0.120 6 25872351 intron variant A/G snv 0.12 0.700 1.000 2 2010 2013
dbSNP: rs11964886
rs11964886
2 0.925 0.120 6 25878151 intron variant C/A;T snv 0.700 1.000 1 2013 2013
dbSNP: rs11969868
rs11969868
2 0.925 0.120 6 25878278 intron variant A/G snv 0.19 0.700 1.000 1 2013 2013
dbSNP: rs1408271
rs1408271
2 0.925 0.120 6 25859393 intron variant T/A snv 0.29 0.700 1.000 1 2013 2013
dbSNP: rs4712976
rs4712976
2 0.925 0.120 6 25841975 intron variant C/T snv 0.26 0.700 1.000 1 2013 2013
dbSNP: rs566530
rs566530
2 0.925 0.120 6 25878133 intron variant T/A;C snv 0.700 1.000 1 2010 2010
dbSNP: rs9467621
rs9467621
2 0.925 0.120 6 25851110 intron variant G/A snv 7.3E-02 0.700 1.000 1 2013 2013
dbSNP: rs9467622
rs9467622
2 0.925 0.120 6 25854416 intron variant C/A;T snv 0.700 1.000 1 2013 2013
dbSNP: rs1165148
rs1165148
3 0.925 0.120 6 25844482 intron variant G/T snv 0.25 0.700 1.000 3 2010 2013
dbSNP: rs1165158
rs1165158
3 0.925 0.120 6 25864670 intron variant C/A snv 0.25 0.700 1.000 3 2010 2013
dbSNP: rs1165159
rs1165159
3 0.925 0.120 6 25864397 intron variant A/G snv 0.25 0.700 1.000 3 2010 2013
dbSNP: rs1165161
rs1165161
3 0.925 0.120 6 25864134 intron variant C/T snv 0.25 0.700 1.000 3 2010 2013
dbSNP: rs1165162
rs1165162
3 0.925 0.120 6 25863377 intron variant C/T snv 0.25 0.700 1.000 3 2010 2013
dbSNP: rs1165164
rs1165164
3 0.925 0.120 6 25863253 intron variant G/A snv 0.24 0.700 1.000 3 2010 2013
dbSNP: rs1165165
rs1165165
3 0.925 0.120 6 25862238 missense variant C/T snv 0.21 0.24 0.700 1.000 3 2010 2013
dbSNP: rs1165167
rs1165167
3 0.925 0.120 6 25860460 intron variant A/G snv 0.25 0.700 1.000 3 2010 2013
dbSNP: rs1165187
rs1165187
3 0.925 0.120 6 25851141 intron variant T/C snv 0.25 0.700 1.000 3 2010 2013