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: rs760539449
rs760539449
1 1.000 0.080 22 37974064 missense variant T/C snv 8.4E-05 5.6E-05 0.700 0
dbSNP: rs1365019464
rs1365019464
1 1.000 0.080 22 37974187 missense variant C/T snv 7.0E-06 0.010 1.000 1 2001 2001