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: rs121912664
rs121912664
31 0.667 0.357 17 7670699 missense variant C/A,G,T snp 1.2E-05 0.760 0.833 19 1998 2017
dbSNP: rs11540654
rs11540654
117 0.492 0.679 17 7676040 missense variant C/A,G,T snp 4.8E-05 3.2E-05 0.730 1.000 15 1997 2017
dbSNP: rs121912651
rs121912651
41 0.618 0.464 17 7674221 missense variant G/A,C snp 4.0E-06 0.720 1.000 24 1991 2017
dbSNP: rs121912666
rs121912666
29 0.647 0.321 17 7674872 missense variant T/C,G snp 8.0E-06 0.720 1.000 19 1994 2017
dbSNP: rs28934576
rs28934576
64 0.563 0.536 17 7673802 missense variant C/A,G,T snp 4.0E-06; 1.6E-05 0.720 1.000 15 1992 2017
dbSNP: rs375338359
rs375338359
6 0.923 0.143 17 7670684 missense variant C/G,T snp 8.0E-06 0.720 1.000 10 1998 2017
dbSNP: rs28934575
rs28934575
25 0.673 0.321 17 7674230 missense variant C/A,G,T snp 0.710 1.000 36 1991 2017
dbSNP: rs587782144
rs587782144
6 0.821 0.143 17 7675139 missense variant C/G,T snp 4.0E-06; 4.0E-06 0.710 1.000 28 1999 2017
dbSNP: rs28934578
rs28934578
27 0.647 0.357 17 7675088 missense variant snp 4.0E-06 0.710 1.000 20 1994 2017
dbSNP: rs397514495
rs397514495
22 0.707 0.286 17 7675070 missense variant C/A,T snp 1.2E-05 3.2E-05 0.710 1.000 19 1992 2017
dbSNP: rs587778720
rs587778720
29 0.647 0.321 17 7674893 missense variant C/A,G,T snp 4.0E-06 0.710 1.000 16 1994 2017
dbSNP: rs137853007
rs137853007
5 0.846 0.179 22 28725254 missense variant G/A,T snp 5.2E-05 3.2E-05 0.710 1.000 4 2001 2012
dbSNP: rs121912655
rs121912655
14 0.724 0.321 17 7674238 missense variant C/A,G,T snp 0.700 19 1989 2017
dbSNP: rs587782705
rs587782705
4 0.878 0.107 17 7675157 missense variant G/A snp 8.0E-06 0.700 18 1994 2017
dbSNP: rs28934574
rs28934574
25 0.667 0.393 17 7673776 missense variant G/A,C snp 4.0E-06 0.700 14 1992 2017
dbSNP: rs121912656
rs121912656
24 0.667 0.500 17 7674229 missense variant C/A,G,T snp 4.0E-06; 4.0E-06 0.700 13 1991 2017
dbSNP: rs730882005
rs730882005
17 0.707 0.393 17 7674250 missense variant C/A,G,T snp 8.0E-06 0.700 13 1994 2017
dbSNP: rs397516435
rs397516435
2 1.000 0.107 17 7674945 stop gained G/A,C snp 4.0E-06 0.700 12 1994 2017
dbSNP: rs397516436
rs397516436
30 0.647 0.393 17 7674894 stop gained G/A,C snp 0.700 12 1994 2017
dbSNP: rs55863639
rs55863639
2 1.000 0.107 17 7675994 splice region variant C/A,T snp 0.700 12 1993 2017
dbSNP: rs587781525
rs587781525
22 0.679 0.429 17 7673778 missense variant T/A,C,G snp 0.700 11 1999 2017
dbSNP: rs1057519989
rs1057519989
15 0.724 0.214 17 7674233 missense variant C/A,G,T snp 0.700 10 2003 2017
dbSNP: rs112431538
rs112431538
5 0.846 0.179 17 7673767 missense variant C/T snp 0.700 10 1997 2017
dbSNP: rs148924904
rs148924904
18 0.707 0.321 17 7675124 stop lost T/C snp 0.700 10 1994 2017
dbSNP: rs587780070
rs587780070
24 0.667 0.286 17 7675077 missense variant G/A,C,T snp 4.0E-06 0.700 10 2002 2017