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: rs121908859
rs121908859
TSHR ; LOC101928462
2 1.000 0.040 14 81143914 missense variant A/G snv 0.700 0
dbSNP: rs121908860
rs121908860
TSHR ; LOC101928462
1 1.000 0.040 14 81143925 missense variant GC/AT mnv 0.700 0
dbSNP: rs121908861
rs121908861
TSHR ; LOC101928462
2 0.925 0.040 14 81143949 missense variant T/C snv 0.700 0
dbSNP: rs121908873
rs121908873
TSHR ; LOC101928462
7 0.790 0.160 14 81139828 missense variant G/A;T snv 0.700 0
dbSNP: rs121908877
rs121908877
TSHR ; LOC101928462
2 0.925 0.040 14 81143945 missense variant G/A;T snv 4.0E-06 0.700 0