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: rs73329476
rs73329476 		2 0.925 0.080 12 69110303 regulatory region variant C/T snv 0.16 0.710 1.000 2 2014 2019
dbSNP: rs1800471
rs1800471
TGFB1
48 0.597 0.840 19 41352971 missense variant C/G;T snv 5.6E-02 0.010 1.000 1 2017 2017
dbSNP: rs1800629
rs1800629
TNF
169 0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14 0.010 1.000 1 2013 2013
dbSNP: rs4320486
rs4320486
LAMB1
1 1.000 0.080 7 108003532 upstream gene variant C/T snv 0.43 0.010 1.000 1 2017 2017