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: rs1042636
rs1042636
23 0.672 0.360 3 122284922 missense variant A/G snv 0.15 9.0E-02 0.010 1.000 1 2008 2008
dbSNP: rs773552397
rs773552397
1 1.000 0.040 3 122284641 missense variant G/A;T snv 8.0E-06; 4.0E-06 0.010 1.000 1 2006 2006