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: rs1204330294
rs1204330294
TSHR ; LOC101928462
1 1.000 0.040 14 81143173 missense variant A/C snv 8.7E-05; 4.0E-06 1.4E-05 0.010 1.000 1 2008 2008
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 1999 1999
dbSNP: rs121908876
rs121908876
TSHR ; LOC101928462
2 0.925 0.040 14 81143572 missense variant G/A snv 0.010 1.000 1 2004 2004
dbSNP: rs121908880
rs121908880
TSHR ; LOC101928462
3 0.882 0.040 14 81143973 missense variant C/T snv 0.010 1.000 1 1999 1999
dbSNP: rs1801252
rs1801252
ADRB1
17 0.724 0.320 10 114044277 missense variant A/G snv 0.15 0.17 0.010 1.000 1 2014 2014
dbSNP: rs1801253
rs1801253
ADRB1
34 0.683 0.440 10 114045297 missense variant G/C snv 0.74 0.69 0.010 1.000 1 2014 2014
dbSNP: rs757110
rs757110
ABCC8
6 0.851 0.080 11 17396930 missense variant C/A;T snv 0.64; 8.0E-06 0.010 1.000 1 2014 2014