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: rs387906861
rs387906861
CRADD
1 1.000 12 93850053 missense variant G/A;C snv 8.0E-06 0.800 1.000 1 2012 2012
dbSNP: rs141179774
rs141179774
CRADD
1 1.000 12 93850180 missense variant G/A snv 5.8E-04 5.2E-04 0.700 0
dbSNP: rs370916968
rs370916968
CRADD
1 1.000 12 93850162 missense variant T/G snv 1.2E-05 4.2E-05 0.700 0
dbSNP: rs749655461
rs749655461
CRADD
1 1.000 12 93850179 missense variant C/T snv 1.2E-05 1.4E-05 0.700 0