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: rs121434441
rs121434441
3 0.882 0.240 12 57569015 missense variant A/G snv 0.800 1.000 8 2002 2011
dbSNP: rs121434442
rs121434442
1 1.000 0.080 12 57569274 missense variant C/T snv 0.800 1.000 8 2002 2011
dbSNP: rs121434443
rs121434443
2 0.925 0.120 12 57569263 missense variant A/G snv 0.800 1.000 8 2002 2011
dbSNP: rs121434444
rs121434444
4 0.882 0.160 12 57569648 missense variant C/T snv 2.8E-05 7.0E-06 0.800 1.000 8 2002 2011
dbSNP: rs387907285
rs387907285
2 0.925 0.120 12 57568999 missense variant G/A snv 0.800 0
dbSNP: rs387907287
rs387907287
2 0.925 0.120 12 57567515 missense variant G/A snv 0.800 0
dbSNP: rs387907288
rs387907288
2 0.925 0.080 12 57569275 missense variant G/A snv 0.800 0
dbSNP: rs1131692233
rs1131692233
1 1.000 0.080 12 57569047 missense variant T/C snv 0.700 0
dbSNP: rs387907289
rs387907289
1 1.000 0.080 12 57567608 missense variant G/A snv 0.700 0
dbSNP: rs690016545
rs690016545
1 1.000 0.080 12 57567598 missense variant G/A snv 0.700 0