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: rs121912456
rs121912456
SOD1 ; LOC102724449
6 0.851 0.120 21 31659806 missense variant G/C snv 0.010 1.000 1 2005 2005
dbSNP: rs774994509
rs774994509
SOD1
5 0.851 0.080 21 31667296 missense variant A/G snv 4.0E-06 0.010 1.000 1 2011 2011
dbSNP: rs1062577
rs1062577
ESR1
4 0.882 0.080 6 152102770 3 prime UTR variant T/A;G snv 0.010 1.000 1 2013 2013
dbSNP: rs483352809
rs483352809
TUBB4A
5 0.882 0.120 19 6495754 missense variant C/T snv 0.010 1.000 1 2014 2014
dbSNP: rs61731956
rs61731956
MADD ; NR1H3
3 0.925 0.080 11 47268596 missense variant G/A snv 2.2E-04 2.6E-04 0.020 1.000 2 2016 2016
dbSNP: rs1405999227
rs1405999227
EGFR
3 0.925 0.160 7 55156637 missense variant A/G snv 4.0E-06 0.010 1.000 1 2018 2018
dbSNP: rs2640
rs2640
EIF2AK1
3 0.925 0.080 7 6026819 missense variant T/C snv 9.0E-02 5.5E-02 0.010 1.000 1 2017 2017
dbSNP: rs391745
rs391745 		3 0.925 0.080 X 97839482 intergenic variant C/G;T snv 0.010 1.000 1 2011 2011
dbSNP: rs471979
rs471979
NLRP5
3 0.925 0.080 19 56027610 missense variant G/C snv 0.13 9.7E-02 0.010 1.000 1 2017 2017
dbSNP: rs58124832
rs58124832
CACNA1H
3 0.925 0.080 16 1218376 missense variant G/A;T snv 5.5E-02 0.010 1.000 1 2017 2017
dbSNP: rs6162
rs6162
CYP17A1
3 0.925 0.080 10 102837224 synonymous variant G/A snv 0.42 0.40 0.010 1.000 1 2013 2013
dbSNP: rs1800876
rs1800876
CMA1
2 1.000 14 24510007 upstream gene variant G/A snv 0.24 0.010 1.000 1 2011 2011
dbSNP: rs7201637
rs7201637
HSD17B2
2 1.000 16 82081670 intron variant T/A snv 9.0E-02 0.010 1.000 1 2013 2013
dbSNP: rs775040765
rs775040765
BRAF
2 1.000 7 140800366 missense variant T/C snv 8.0E-05 1.4E-05 0.010 1.000 1 2018 2018
dbSNP: rs877610
rs877610
TRPV1
3 1.000 17 3572196 synonymous variant C/T snv 4.6E-02 7.5E-02 0.010 1.000 1 2013 2013