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: rs11127129
rs11127129
1 2 27853841 intron variant C/A;G snv 0.700 1.000 1 2012 2012
dbSNP: rs13030345
rs13030345
3 0.925 0.120 2 27780307 intron variant G/T snv 0.15 0.700 1.000 1 2012 2012
dbSNP: rs2305929
rs2305929
4 1.000 0.040 2 27891044 intron variant A/G snv 0.14 0.700 1.000 1 2012 2012
dbSNP: rs3792253
rs3792253
1 2 27779135 intron variant T/C snv 0.22 0.700 1.000 1 2012 2012
dbSNP: rs4666014
rs4666014
2 2 27796308 intron variant G/A snv 0.36 0.700 1.000 1 2012 2012
dbSNP: rs6708889
rs6708889
1 2 27884825 intron variant C/T snv 0.71 0.700 1.000 1 2012 2012
dbSNP: rs898034
rs898034
1 2 27867953 intron variant T/C snv 0.69 0.700 1.000 1 2012 2012