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: rs121918499
rs121918499
2 0.923 0.143 10 121520048 missense variant C/A,G snp 0.830 1.000 7 1997 2011
dbSNP: rs121909627
rs121909627
8 0.769 0.179 8 38424690 missense variant G/C snp 4.0E-06 0.750 1.000 5 2000 2015
dbSNP: rs121918488
rs121918488
6 0.801 0.107 10 121517379 missense variant A/C,G,T snp 0.720 1.000 3 1999 2016
dbSNP: rs121918510
rs121918510
1 1.000 0.071 10 121517441 missense variant T/G snp 0.710 1.000 2 1995 2005
dbSNP: rs121918502
rs121918502
4 0.878 0.107 10 121517351 stop gained G/C snp 0.710 1.000 1 1998 1998
dbSNP: rs776587763
rs776587763
5 0.821 0.071 10 121520085 missense variant C/A,T snp 4.0E-06; 4.0E-06 0.710 1.000 1 2001 2001
dbSNP: rs1057519047
rs1057519047
1 1.000 0.071 10 121488055 missense variant T/C snp 0.700 2 2002 2007
dbSNP: rs121918506
rs121918506
3 0.878 0.071 10 121496701 missense variant T/C,G snp 0.700 2 2002 2007
dbSNP: rs121913478
rs121913478
10 0.756 0.321 10 121515280 missense variant T/C snp 0.700 0
dbSNP: rs121918487
rs121918487
4 0.846 0.071 10 121517378 missense variant C/A,G,T snp 0.700 0
dbSNP: rs121918495
rs121918495
2 0.923 0.071 10 121517382 missense variant T/G snp 0.700 0
dbSNP: rs79184941
rs79184941
29 0.638 0.321 10 121520163 missense variant G/A,C snp 5.6E-05; 4.0E-06 3.2E-05 0.700 0
dbSNP: rs77543610
rs77543610
14 0.724 0.071 10 121520160 missense variant G/C snp 0.030 1.000 3 1998 2004
dbSNP: rs121918498
rs121918498
5 0.846 0.071 10 121520162 missense variant CG/AA multinucleotide-polymorphism 0.010 1.000 1 1997 1997
dbSNP: rs121918501
rs121918501
3 0.878 0.071 10 121520050 missense variant A/C,G snp 0.010 1.000 1 2006 2006
dbSNP: rs374608214
rs374608214
8 0.769 0.071 10 121520010 missense variant G/C snp 4.0E-06 0.010 1.000 1 2004 2004
dbSNP: rs4647924
rs4647924
20 0.715 0.179 4 1801844 missense variant C/A,G,T snp 4.2E-06; 4.2E-06 3.2E-05; 3.2E-05 0.010 1.000 1 2004 2004
dbSNP: rs766812325
rs766812325
4 0.846 0.071 6 45492058 missense variant C/G snp 0.010 1.000 1 2000 2000