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: rs137852952
rs137852952
2 1.000 0.080 4 166003471 missense variant T/C snv 2.1E-04 2.4E-04 0.010 1.000 1 2009 2009
dbSNP: rs375349466
rs375349466
1 4 166003545 missense variant A/G snv 8.0E-06 2.8E-05 0.010 1.000 1 2016 2016