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: rs1057519721
rs1057519721
4 0.882 0.120 9 5078360 missense variant A/G snv 0.700 1.000 4 2008 2012
dbSNP: rs1057519722
rs1057519722
1 1.000 0.120 9 5078361 missense variant G/C snv 4.0E-06 0.700 1.000 4 2008 2012
dbSNP: rs1057519723
rs1057519723
2 0.925 0.120 9 5078362 missense variant A/C;G;T snv 0.700 1.000 4 2008 2012