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: rs35619497
rs35619497
3 0.878 0.107 10 86921680 missense variant C/T snp 6.8E-04 3.8E-04 0.700 2 2003 2007
dbSNP: rs199476086
rs199476086
5 0.846 0.107 10 86919316 missense variant C/A,T snp 0.700 1 2001 2001
dbSNP: rs199476087
rs199476087
4 0.878 0.107 10 86899830 missense variant T/C snp 0.700 1 2001 2001
dbSNP: rs199476088
rs199476088
3 0.878 0.107 10 86919430 missense variant G/A snp 0.700 1 2001 2001
dbSNP: rs199476089
rs199476089
3 0.878 0.107 10 86923442 missense variant T/C snp 0.700 1 2003 2003
dbSNP: rs281875324
rs281875324
5 0.878 0.107 18 51065456 missense variant A/C,G snp 0.700 1 2003 2003
dbSNP: rs80338963
rs80338963
12 0.756 0.250 18 51065548 missense variant C/A,G,T snp 0.700 1 1998 1998
dbSNP: rs121912581
rs121912581
4 0.846 0.179 18 51065521 missense variant G/A snp 0.700 0