Source: BEFREE

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: rs377767404
rs377767404
RET
0.742 0.160 10 43114488 missense variant T/C snv
CUI: C0238462
Disease: Medullary carcinoma of thyroid
Medullary carcinoma of thyroid 		0.730 1.000 3 1999 2017
dbSNP: rs377767404
rs377767404
RET
0.742 0.160 10 43114488 missense variant T/C snv
CUI: C0342190
Disease: C-cell hyperplasia of thyroid
C-cell hyperplasia of thyroid 		0.010 1.000 1 2004 2004
dbSNP: rs377767404
rs377767404
RET
0.742 0.160 10 43114488 missense variant T/C snv
CUI: C1833921
Disease: Familial medullary thyroid carcinoma
Familial medullary thyroid carcinoma 		0.010 1.000 1 2004 2004
dbSNP: rs377767404
rs377767404
RET
0.742 0.160 10 43114488 missense variant T/C snv
CUI: C4551683
Disease: Adrenal Gland Pheochromocytoma
Adrenal Gland Pheochromocytoma 		0.010 1.000 1 2005 2005
dbSNP: rs377767404
rs377767404
RET
0.742 0.160 10 43114488 missense variant T/C snv
CUI: C0020502
Disease: Hyperparathyroidism
Hyperparathyroidism 		0.010 1.000 1 2005 2005
dbSNP: rs377767404
rs377767404
RET
0.742 0.160 10 43114488 missense variant T/C snv
CUI: C0031511
Disease: Pheochromocytoma
Pheochromocytoma 		0.010 1.000 1 2005 2005