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: rs387907178
rs387907178
1 1.000 0.040 1 109548838 missense variant G/A;C snv 0.800 1.000 1 2012 2012
dbSNP: rs387907179
rs387907179
2 0.925 0.040 20 9384333 missense variant A/C;G snv 0.700 1.000 1 2012 2012
dbSNP: rs397514480
rs397514480
2 0.925 0.040 20 9409086 missense variant A/G snv 0.700 1.000 1 2012 2012
dbSNP: rs397514481
rs397514481
5 0.882 0.040 20 9409080 missense variant G/A;T snv 0.700 1.000 1 2012 2012
dbSNP: rs397514482
rs397514482
2 0.925 0.040 20 9409079 missense variant C/A;T snv 4.1E-06 0.700 1.000 1 2012 2012
dbSNP: rs397514483
rs397514483
2 0.925 0.040 20 9409166 missense variant A/C snv 0.700 1.000 1 2012 2012
dbSNP: rs397514768
rs397514768
1 1.000 0.040 1 109573759 missense variant C/A snv 0.700 0