Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs113488022
rs113488022
BRAF
0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06
CUI: C2931367
Disease: Thyroid cancer, follicular
Thyroid cancer, follicular 		0.020 1.000 2 2007 2010
dbSNP: rs121913377
rs121913377
BRAF
0.354 0.840 7 140753335 missense variant CA/AT;TT mnv
CUI: C2931367
Disease: Thyroid cancer, follicular
Thyroid cancer, follicular 		0.020 1.000 2 2007 2010
dbSNP: rs17849071
rs17849071
PIK3CA
0.776 0.160 3 179218439 intron variant T/G snv 7.9E-02
CUI: C2931367
Disease: Thyroid cancer, follicular
Thyroid cancer, follicular 		0.020 1.000 2 2012 2014
dbSNP: rs121908874
rs121908874
TSHR ; LOC101928462
0.807 0.080 14 81143584 missense variant T/C snv
CUI: C2931367
Disease: Thyroid cancer, follicular
Thyroid cancer, follicular 		0.010 1.000 1 2005 2005
dbSNP: rs752021744
rs752021744
PIK3CB
0.689 0.440 3 138759306 missense variant T/C snv 1.2E-05
CUI: C2931367
Disease: Thyroid cancer, follicular
Thyroid cancer, follicular 		0.010 1.000 1 2013 2013