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: rs121908864
rs121908864
TSHR ; LOC101928462
6 0.851 0.120 14 81143416 missense variant T/C;G snv 4.0E-06 0.010 1.000 1 1998 1998
dbSNP: rs121908874
rs121908874
TSHR ; LOC101928462
7 0.807 0.080 14 81143584 missense variant T/C snv 0.010 1.000 1 2005 2005
dbSNP: rs571893270
rs571893270
TSHR ; LOC101928462
3 0.882 0.040 14 81143641 missense variant G/A snv 8.0E-05 2.1E-05 0.010 1.000 1 1998 1998