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: rs121907927
rs121907927
3 0.878 0.071 11 31794072 missense variant C/G snp 4.0E-06 0.700 2 2002 2006
dbSNP: rs121907928
rs121907928
3 0.878 0.071 11 31801561 missense variant G/A,C,T snp 0.700 2 1997 2001
dbSNP: rs121907919
rs121907919
3 0.923 0.071 11 31800837 missense variant A/T snp 0.700 1 1999 1999
dbSNP: rs200015827
rs200015827
2 0.923 0.071 11 31790769 missense variant G/C,T snp 4.0E-06; 2.6E-04 6.4E-05 0.700 1 2001 2001
dbSNP: rs373661718
rs373661718
2 0.923 0.071 11 31790836 missense variant A/C snp 0.700 1 1997 1997
dbSNP: rs749244084
rs749244084
2 0.923 0.071 11 31794689 missense variant C/T snp 8.0E-06 0.700 1 1999 1999
dbSNP: rs757259413
rs757259413
4 0.846 0.071 11 31794690 missense variant G/A snp 4.0E-06 0.700 1 1993 1993
dbSNP: rs780356070
rs780356070
2 0.923 0.071 11 31789938 missense variant T/C snp 4.5E-06 0.700 0
dbSNP: rs121907917
rs121907917
3 0.878 0.071 11 31794079 stop gained G/A snp 0.010 1.000 1 2009 2009