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: rs281865238
rs281865238
3 0.878 0.071 11 61957402 missense variant C/A,T snp 0.700 4 1999 2008
dbSNP: rs28940273
rs28940273
3 0.878 0.071 11 61955749 missense variant G/A,C snp 0.700 4 1998 2016
dbSNP: rs1805144
rs1805144
3 0.878 0.071 11 61959530 missense variant G/C snp 4.0E-06 0.700 3 1999 2003
dbSNP: rs28940274
rs28940274
3 0.878 0.071 11 61955723 missense variant T/C snp 0.700 3 1998 2011
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: 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: rs28940275
rs28940275
3 0.878 0.071 11 61951822 missense variant A/C snp 0.700 2 1998 2009
dbSNP: rs28941469
rs28941469
3 0.878 0.071 11 61957429 missense variant T/A snp 0.700 2 1998 2009
dbSNP: rs1800995
rs1800995
3 0.878 0.071 11 61955906 missense variant GC/AA multinucleotide-polymorphism 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
dbSNP: rs281865209
rs281865209
3 0.878 0.071 11 61951844 missense variant G/A,C snp 1.2E-05 3.2E-05 0.700 1 1999 1999
dbSNP: rs281865210
rs281865210
3 0.878 0.071 11 61951853 missense variant C/T snp 0.700 1 2001 2001
dbSNP: rs281865211
rs281865211
3 0.878 0.071 11 61951856 missense variant T/G snp 0.700 1 2001 2001
dbSNP: rs281865217
rs281865217
3 0.878 0.071 11 61951891 missense variant T/C snp 4.0E-06 0.700 1 2004 2004
dbSNP: rs281865225
rs281865225
4 0.846 0.071 11 61955745 missense variant G/A snp 0.700 1 2001 2001
dbSNP: rs281865226
rs281865226
3 0.878 0.071 11 61955758 missense variant G/C snp 0.700 1 1999 1999
dbSNP: rs281865230
rs281865230
3 0.878 0.071 11 61955774 missense variant T/C snp 0.700 1 2004 2004
dbSNP: rs281865231
rs281865231
3 0.878 0.071 11 61955780 missense variant G/C snp 0.700 1 2004 2004
dbSNP: rs281865234
rs281865234
3 0.878 0.071 11 61955873 missense variant G/A snp 0.700 1 1999 1999
dbSNP: rs281865239
rs281865239
4 0.846 0.071 11 61957403 missense variant G/A snp 1.2E-05 0.700 1 2001 2001
dbSNP: rs281865240
rs281865240
3 0.878 0.071 11 61957413 missense variant T/G snp 0.700 1 2000 2000
dbSNP: rs281865243
rs281865243
3 0.878 0.071 11 61957421 missense variant T/A,C snp 0.700 1 2000 2000