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: rs10211196
rs10211196
1 2 203265173 intron variant G/A snv 0.40 0.700 1.000 1 2011 2011
dbSNP: rs11693128
rs11693128
1 2 203251178 intron variant A/G snv 0.44 0.700 1.000 1 2011 2011
dbSNP: rs12693984
rs12693984
1 2 203287810 intron variant C/T snv 0.39 0.700 1.000 1 2011 2011
dbSNP: rs2043444
rs2043444
1 2 203278403 intron variant T/A;C snv 0.700 1.000 1 2011 2011
dbSNP: rs3731694
rs3731694
1 2 203251937 intron variant A/T snv 0.50 0.700 1.000 1 2011 2011
dbSNP: rs4675324
rs4675324
1 2 203242302 intron variant G/A snv 0.39 0.700 1.000 1 2011 2011
dbSNP: rs7606820
rs7606820
1 2 203270547 intron variant A/G;T snv 0.700 1.000 1 2011 2011