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: rs769346296
rs769346296
PRNP
1 1.000 0.120 20 4699807 missense variant A/C snv 6.0E-05 2.8E-05 0.030 1.000 3 2014 2019
dbSNP: rs1799990
rs1799990
PRNP
23 0.683 0.440 20 4699605 missense variant A/G snv 0.31 0.33 0.900 1.000 14 1996 2015
dbSNP: rs1290309353
rs1290309353
AZIN2
3 0.882 0.120 1 33096833 missense variant A/G snv 4.0E-06 0.010 1.000 1 2010 2010
dbSNP: rs16840647
rs16840647
RGS7
1 1.000 0.120 1 240799770 intron variant A/G snv 4.1E-02 0.700 1.000 1 2012 2012
dbSNP: rs16990018
rs16990018
PRNP
5 0.882 0.120 20 4699732 missense variant A/G snv 3.8E-03 1.6E-02 0.010 1.000 1 2010 2010
dbSNP: rs63751249
rs63751249
MAPT
1 1.000 0.120 17 45996620 missense variant A/G snv 0.010 1.000 1 2017 2017
dbSNP: rs74315413
rs74315413
PRNP
8 0.807 0.160 20 4699780 missense variant A/G snv 0.010 1.000 1 2004 2004
dbSNP: rs748929962
rs748929962
PRNP
1 1.000 0.120 20 4699894 missense variant A/G snv 4.0E-06 0.010 1.000 1 2019 2019
dbSNP: rs11538758
rs11538758
PRNP
8 0.882 0.160 20 4699534 missense variant C/A;T snv 0.010 1.000 1 2013 2013
dbSNP: rs140842009
rs140842009
GPI
3 0.882 0.120 19 34378959 missense variant C/A;T snv 4.0E-06; 5.2E-05 0.010 1.000 1 2008 2008
dbSNP: rs35453518
rs35453518
PRND
1 1.000 0.120 20 4724718 missense variant C/A;T snv 8.0E-06; 8.1E-03 0.010 1.000 1 2004 2004
dbSNP: rs41279424
rs41279424
PRND
1 1.000 0.120 20 4724628 missense variant C/A;T snv 2.4E-05; 2.0E-02 0.010 1.000 1 2004 2004
dbSNP: rs75932628
rs75932628
TREM2 ; LOC105375056
28 0.662 0.480 6 41161514 missense variant C/A;T snv 6.8E-05; 2.6E-03 0.010 1.000 1 2014 2014
dbSNP: rs638405
rs638405
BACE1 ; BACE1-AS
4 0.851 0.160 11 117293108 synonymous variant C/G snv 0.49 0.46 0.010 1.000 1 2012 2012
dbSNP: rs2245220
rs2245220
PRND
3 0.882 0.160 20 4725072 missense variant C/G;T snv 4.1E-06; 0.46 0.52 0.010 < 0.001 1 2004 2004
dbSNP: rs753438778
rs753438778
CSF2
2 0.925 0.160 5 132074925 missense variant C/G;T snv 8.0E-06; 4.0E-06 0.010 1.000 1 2013 2013
dbSNP: rs74315401
rs74315401
PRNP
32 0.683 0.320 20 4699525 missense variant C/T snv 0.040 1.000 4 1995 2013
dbSNP: rs1191139947
rs1191139947
PRNP
3 0.882 0.120 20 4699935 missense variant C/T snv 0.010 1.000 1 2008 2008
dbSNP: rs74315402
rs74315402
PRNP
7 0.882 0.200 20 4699570 missense variant C/T snv 0.010 1.000 1 2009 2009
dbSNP: rs773268484
rs773268484
AQP1
4 0.851 0.120 7 30922174 frameshift variant G/- delins 4.0E-06 7.0E-06 0.010 1.000 1 2019 2019
dbSNP: rs28933385
rs28933385
PRNP
25 0.695 0.320 20 4699818 missense variant G/A snv 4.0E-06 0.900 1.000 44 1990 2019
dbSNP: rs74315408
rs74315408
PRNP
16 0.752 0.280 20 4699758 missense variant G/A snv 6.4E-05 4.2E-05 0.900 1.000 27 1990 2019
dbSNP: rs74315403
rs74315403
PRNP
10 0.790 0.200 20 4699752 missense variant G/A snv 0.800 0.955 22 1990 2015
dbSNP: rs74315407
rs74315407
PRNP
15 0.732 0.240 20 4699848 missense variant G/A snv 8.0E-06 2.1E-05 0.870 1.000 18 1990 2016
dbSNP: rs74315412
rs74315412
PRNP
5 0.851 0.120 20 4699843 missense variant G/A snv 6.0E-05 3.5E-05 0.750 1.000 16 1990 2014