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: rs137852643
rs137852643
3 0.925 0.080 7 30609729 missense variant G/C snv 4.0E-06 0.800 1.000 9 2003 2015
dbSNP: rs137852645
rs137852645
2 0.925 0.080 7 30599996 missense variant A/G snv 0.800 1.000 9 2003 2015
dbSNP: rs137852647
rs137852647
2 0.925 0.080 7 30626280 missense variant G/A snv 2.0E-05 7.0E-06 0.800 1.000 9 2003 2015
dbSNP: rs137852648
rs137852648
1 1.000 0.080 7 30612107 missense variant C/T snv 0.800 1.000 9 2003 2015
dbSNP: rs1554337974
rs1554337974
3 0.882 0.080 7 30609643 missense variant C/T snv 0.700 1.000 9 2003 2015
dbSNP: rs1554338260
rs1554338260
2 0.925 0.080 7 30612214 missense variant A/T snv 0.700 1.000 9 2003 2015
dbSNP: rs370531212
rs370531212
2 0.925 0.080 7 30599954 missense variant C/T snv 1.4E-05 0.700 1.000 9 2003 2015
dbSNP: rs201358272
rs201358272
2 0.925 0.080 7 30632247 missense variant C/G;T snv 4.0E-06; 2.0E-04 0.700 1.000 6 2006 2016
dbSNP: rs863224873
rs863224873
2 0.925 0.080 7 30612212 missense variant A/C;G;T snv 0.700 0