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: rs1237473071
rs1237473071
TSHR ; LOC101928462
2 0.925 0.040 14 81143791 missense variant T/C snv 7.0E-06 0.010 1.000 1 2012 2012
dbSNP: rs2069566
rs2069566
TG ; LOC105375768
4 0.851 0.160 8 133017940 missense variant G/A snv 8.0E-06 2.1E-05 0.010 1.000 1 2010 2010