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: rs11126184
rs11126184 		2 0.925 0.080 2 68425042 intergenic variant C/A snv 0.55 0.010 1.000 1 2012 2012
dbSNP: rs5370
rs5370
EDN1
37 0.630 0.520 6 12296022 missense variant G/T snv 0.23 0.21 0.010 1.000 1 2009 2009
dbSNP: rs7030789
rs7030789
LPAR1
3 0.925 0.080 9 110973232 intron variant A/G snv 0.68 0.010 1.000 1 2012 2012