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: rs1695
rs1695
100 0.510 0.679 11 67585218 missense variant A/G snp 0.34 0.35 0.010 1.000 1 2008 2008
dbSNP: rs17563
rs17563
2 1.000 14 53950804 stop lost A/G snp 0.45 0.47 0.010 1.000 1 2017 2017
dbSNP: rs2235371
rs2235371
3 0.878 0.107 1 209790735 missense variant C/T snp 8.7E-02 3.8E-02 0.010 1.000 1 2006 2006
dbSNP: rs397507444
rs397507444
169 0.457 0.714 1 11794407 missense variant T/G snp 0.010 < 0.001 1 2003 2003
dbSNP: rs6576618
rs6576618
1 1.000 15 26799458 intron variant A/C snp 0.59 0.010 1.000 1 2013 2013
dbSNP: rs981778
rs981778
1 1.000 15 26712093 intron variant G/A snp 0.32 0.010 1.000 1 2013 2013