Source: ALL
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: rs1800802
rs1800802
MGP ; C12orf60
3 0.925 0.040 12 14885985 intron variant A/G snv 0.15 0.010 1.000 1 2017 2017
dbSNP: rs4236
rs4236
MGP ; C12orf60
4 0.925 0.120 12 14882147 missense variant T/A;C snv 0.37 0.010 1.000 1 2017 2017
dbSNP: rs4918
rs4918
AHSG
12 0.763 0.400 3 186620593 missense variant G/A;C snv 0.67 0.010 1.000 1 2009 2009