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: rs28940274
rs28940274
3 0.878 0.071 11 61955723 missense variant T/C snp 0.810 1.000 4 1998 2012
dbSNP: rs281865238
rs281865238
3 0.878 0.071 11 61957402 missense variant C/A,T snp 0.800 5 1999 2014
dbSNP: rs28940273
rs28940273
3 0.878 0.071 11 61955749 missense variant G/A,C snp 0.800 5 1977 2016
dbSNP: rs28940275
rs28940275
3 0.878 0.071 11 61951822 missense variant A/C snp 0.800 4 1998 2009
dbSNP: rs28941469
rs28941469
3 0.878 0.071 11 61957429 missense variant T/A snp 0.800 4 1964 2009
dbSNP: rs28940570
rs28940570
3 0.878 0.071 11 61958159 missense variant C/T snp 4.0E-06 0.800 3 2000 2014
dbSNP: rs1800995
rs1800995
3 0.878 0.071 11 61955906 missense variant GC/AA multinucleotide-polymorphism 0.800 1 1999 1999
dbSNP: rs28940276
rs28940276
3 0.878 0.071 11 61951831 missense variant G/A snp 0.800 1 1998 1998
dbSNP: rs28940278
rs28940278
3 0.878 0.071 11 61951946 missense variant G/A snp 1.6E-05 0.800 1 2000 2000
dbSNP: rs28941468
rs28941468
3 0.878 0.071 11 61959526 missense variant G/A snp 0.800 1 1998 1998
dbSNP: rs281865239
rs281865239
4 0.846 0.071 11 61957403 missense variant G/A snp 1.2E-05 0.710 1.000 2 2001 2016
dbSNP: rs281865267
rs281865267
3 0.878 0.071 11 61959548 missense variant G/C snp 0.710 1.000 2 2000 2016
dbSNP: rs121918284
rs121918284
4 0.846 0.071 11 61955892 missense variant G/A snp 5.2E-04 5.7E-04 0.710 1.000 1 2012 2012
dbSNP: rs281865214
rs281865214
3 0.878 0.071 11 61951879 missense variant C/A,G,T snp 3.2E-05; 4.0E-06; 4.0E-06 6.4E-05 0.710 1.000 1 2013 2013
dbSNP: rs1805144
rs1805144
3 0.878 0.071 11 61959530 missense variant G/C snp 4.0E-06 0.700 3 1999 2003
dbSNP: rs1805143
rs1805143
3 0.878 0.071 11 61959519 missense variant C/G,T snp 4.0E-06 0.700 2 1999 2003
dbSNP: rs267606677
rs267606677
2 0.923 0.071 11 61957430 missense variant A/G snp 0.700 2 1998 2009
dbSNP: rs281865224
rs281865224
3 0.878 0.071 11 61955744 missense variant C/A,T snp 3.2E-05 0.700 2 1999 2008
dbSNP: rs281865530
rs281865530
3 0.878 0.071 11 61955198 missense variant C/G,T snp 2.4E-05 0.700 2 1999 2009
dbSNP: rs121918283
rs121918283
1 1.000 0.071 11 61959513 inframe deletion CATC/C in-del 0.700 1 1998 1998
dbSNP: rs121918285
rs121918285
1 1.000 0.071 11 61951893 stop gained C/G,T snp 4.0E-06 0.700 1 2006 2006
dbSNP: rs1805142
rs1805142
1 1.000 0.071 11 61955825 missense variant G/C,T snp 2.7E-05 3.2E-05 0.700 1 1999 1999
dbSNP: rs199529046
rs199529046
3 0.878 0.071 11 61956964 missense variant T/C,G snp 6.8E-05 6.4E-05 0.700 1 2000 2000
dbSNP: rs281865207
rs281865207
4 0.878 0.071 11 61951835 missense variant C/T snp 0.700 1 1999 1999
dbSNP: rs281865208
rs281865208
3 0.878 0.071 11 61951838 missense variant A/G,T snp 4.0E-06 0.700 1 2004 2004