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: rs63750756
rs63750756
18 0.734 0.107 17 46010324 missense variant T/G snp 2.6E-05 0.730 1.000 7 1998 2007
dbSNP: rs63751273
rs63751273
26 0.692 0.250 17 46010389 missense variant C/T snp 0.700 5 1998 1999
dbSNP: rs63750376
rs63750376
8 0.784 0.107 17 45996657 missense variant G/T snp 0.700 2 1998 1999
dbSNP: rs63750416
rs63750416
5 0.846 0.107 17 46010373 missense variant A/C snp 0.700 2 2002 2002
dbSNP: rs63750570
rs63750570
7 0.821 0.107 17 46018629 missense variant G/A snp 0.700 2 1998 1999
dbSNP: rs63750092
rs63750092
5 0.821 0.107 17 46014277 missense variant A/T snp 0.700 1 2006 2006
dbSNP: rs63750349
rs63750349
5 0.821 0.107 17 45996638 missense variant C/G,T snp 4.0E-06 0.700 1 2004 2004
dbSNP: rs63750711
rs63750711
4 0.846 0.107 17 46018645 missense variant A/T snp 0.700 1 2001 2001
dbSNP: rs63750959
rs63750959
7 0.784 0.179 17 45962351 missense variant G/A,T snp 6.0E-05 0.700 1 2002 2002
dbSNP: rs63751165
rs63751165
5 0.846 0.107 17 46010401 missense variant G/A snp 0.700 1 1999 1999
dbSNP: rs63751399
rs63751399
6 0.801 0.107 14 73171047 missense variant T/C snp 0.700 1 2001 2001
dbSNP: rs63751438
rs63751438
12 0.784 0.107 17 46010388 missense variant C/T snp 0.700 0