Source: BEFREE ×
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: rs104894161
rs104894161
EGR2
3 0.807 0.080 10 62813563 missense variant G/A snv 0.830 1.000 3 1999 2005
dbSNP: rs121913586
rs121913586
MPZ
2 0.752 0.200 1 161306414 missense variant C/G;T snv 0.810 1.000 1 1993 2003
dbSNP: rs104894621
rs104894621
PMP22
4 0.790 0.080 17 15239575 missense variant G/A snv 0.720 1.000 2 1993 2004
dbSNP: rs104894624
rs104894624
PMP22
1 0.925 0.080 17 15230952 missense variant C/A;G;T snv 4.0E-06 0.710 1.000 1 1993 2002
dbSNP: rs104894708
rs104894708
PRX
2 0.851 0.120 19 40395144 stop gained G/A snv 8.0E-06 0.710 1.000 1 2001 2016
dbSNP: rs121913585
rs121913585
MPZ
1 0.851 0.080 1 161307304 missense variant G/A;C snv 0.710 1.000 1 1993 2003
dbSNP: rs121913590
rs121913590
MPZ
4 0.851 0.080 1 161306864 missense variant G/A snv 7.0E-06 0.710 1.000 1 1993 2010
dbSNP: rs121913595
rs121913595
MPZ
4 0.742 0.160 1 161306785 missense variant G/A;T snv 0.710 1.000 1 2010 2010
dbSNP: rs1553259707
rs1553259707
MPZ
1 0.851 0.080 1 161306911 missense variant T/C snv 0.710 1.000 1 1993 2003
dbSNP: rs775019409
rs775019409
PMP22
1 1.000 0.080 17 15230953 missense variant G/A;T snv 8.0E-06 0.710 1.000 1 2000 2000
dbSNP: rs104894159
rs104894159
EGR2
3 0.827 0.080 10 62813413 missense variant G/A snv 0.030 1.000 3 1999 2005
dbSNP: rs281865121
rs281865121
MPZ
1 0.925 0.080 1 161307403 missense variant A/G snv 0.030 1.000 3 2007 2015
dbSNP: rs3132468
rs3132468
MICB
5 0.827 0.240 6 31507709 intron variant C/T snv 0.77 0.020 0.500 2 2013 2014
dbSNP: rs10425452
rs10425452
PRX
1 1.000 0.080 19 40397853 missense variant G/A snv 1.6E-04 6.1E-04 0.010 1.000 1 2013 2013
dbSNP: rs1143627
rs1143627
IL1B
45 0.605 0.760 2 112836810 5 prime UTR variant G/A snv 0.56 0.010 1.000 1 2014 2014
dbSNP: rs121913597
rs121913597
MPZ
2 0.827 0.160 1 161307268 missense variant T/A snv 0.010 1.000 1 2010 2010
dbSNP: rs121913601
rs121913601
MPZ
2 0.851 0.080 1 161307259 missense variant G/A;C snv 0.010 1.000 1 1998 1998
dbSNP: rs1800875
rs1800875
CMA1
12 0.742 0.360 14 24510132 upstream gene variant C/T snv 0.41 0.010 < 0.001 1 2015 2015
dbSNP: rs1801274
rs1801274
FCGR2A
41 0.597 0.800 1 161509955 missense variant A/C;G snv 4.0E-06; 0.48 0.010 1.000 1 2015 2015
dbSNP: rs3740360
rs3740360
PLCE1
5 0.827 0.240 10 94265734 intron variant A/C snv 9.7E-02 8.4E-02 0.010 < 0.001 1 2013 2013
dbSNP: rs3765524
rs3765524
PLCE1
15 0.724 0.320 10 94298541 missense variant C/T snv 0.27 0.31 0.010 1.000 1 2014 2014
dbSNP: rs530552002
rs530552002
MAD2L1BP
1 1.000 0.080 6 43636471 missense variant C/T snv 4.0E-06 0.010 1.000 1 1998 1998
dbSNP: rs753586692
rs753586692
IL4R
1 1.000 0.080 16 27352579 missense variant C/T snv 5.2E-05 5.6E-05 0.010 1.000 1 2013 2013
dbSNP: rs765108575
rs765108575
MAD2L1BP
1 1.000 0.080 6 43636483 missense variant G/A snv 4.0E-06; 4.0E-06 1.4E-05 0.010 1.000 1 1998 1998
dbSNP: rs770546306
rs770546306
MPZ
1 0.882 0.080 1 161307402 missense variant G/A;C;T snv 3.2E-05; 5.2E-05 0.010 1.000 1 2015 2015