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: rs144526169
rs144526169
PROS1
2 1.000 3 93910681 missense variant C/T snv 3.4E-04 3.9E-04 0.700 1.000 1 2019 2019
dbSNP: rs5017717
rs5017717
PROS1
1 3 93884869 stop gained G/A snv 0.700 1.000 1 2019 2019
dbSNP: rs6122
rs6122
PROS1
3 0.925 3 93927251 missense variant G/A snv 5.2E-05 2.8E-05 0.700 1.000 1 2019 2019