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: rs1555572829
rs1555572829
1 1.000 17 47292251 missense variant A/G snv 0.700 0
dbSNP: rs202229101
rs202229101
GP9
2 0.925 3 129062107 missense variant C/T snv 9.5E-04 8.7E-04 0.010 1.000 1 2017 2017