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: rs28939072
rs28939072
2 0.925 0.040 14 91891334 missense variant A/G snv 0.010 1.000 1 2010 2010
dbSNP: rs121434303
rs121434303
3 0.882 0.120 14 91870336 missense variant C/T snv 0.010 1.000 1 2006 2006
dbSNP: rs28939370
rs28939370
3 0.882 0.120 14 91887253 missense variant A/G snv 0.010 1.000 1 2010 2010
dbSNP: rs80338766
rs80338766
3 0.882 0.120 14 91887283 missense variant A/G snv 0.010 1.000 1 2006 2006
dbSNP: rs149396611
rs149396611
4 0.851 0.120 14 91883017 missense variant C/T snv 2.6E-04 2.5E-04 0.010 1.000 1 2010 2010