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rs387906391(CCT;CCT)

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common in clinvar

Is a	genotype
of	rs387906391
Gene	ACVRL1
Chromosome	12
Position	51,914,508
Merged from	Rs878853415
mentioned	by

0

Good

Geno	Mag	Summary
(-;CCT)	4
(-;CTC)	4.3	Hereditary hemorrhagic telangiectasia
(CCT;CCT)	0	common in clinvar
(CTC;CTC)	0	common in clinvar

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Is a genotype