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: rs34637584
rs34637584
LRRK2
47 0.630 0.321 12 40340400 missense variant G/A snp 5.3E-04 1.9E-04 0.020 1.000 2 2010 2015
dbSNP: rs10772715
rs10772715
GRIN2B
2 12 13885069 intron variant G/A snp 0.38 0.010 1.000 1 2013 2013
dbSNP: rs11866328
rs11866328
GRIN2A
3 0.923 0.107 16 9768699 intron variant G/T snp 0.37 0.010 1.000 1 2013 2013
dbSNP: rs2192970
rs2192970
GRIN2B
2 12 13683379 intron variant G/A snp 0.14 0.010 1.000 1 2013 2013