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: rs267607038
rs267607038
2 0.882 0.320 18 44951952 missense variant T/C;G snv 8.0E-06 0.800 1.000 1 2010 2017
dbSNP: rs267607039
rs267607039
1 1.000 0.240 18 44951949 missense variant G/A snv 0.800 1.000 1 2010 2010
dbSNP: rs267607040
rs267607040
4 0.851 0.320 18 44951948 missense variant G/A snv 0.800 1.000 1 2010 2010
dbSNP: rs267607041
rs267607041
1 1.000 0.240 18 44951943 missense variant A/C snv 0.800 1.000 1 2010 2010
dbSNP: rs267607042
rs267607042
4 0.851 0.320 18 44951942 missense variant G/A;C snv 0.800 1.000 1 2010 2017