Individual ID: 15667538.01

Individual ID	15667538.01
Pubmed ID	15667538
Whose mosaic mutation	Father
Phenotypic Category	2
Age	1.0
Number of affected children	1 ( male: 1; )
Disease	May Hegglin anomaly(view all the variants in this disease)
OMIM ID	155100

Variants

Found 3 variants in this database.

Variant ID	Entrez Gene ID	Gene	Chromsome	Start	End	Disease	Method
492	4627	MYH9	22	36678779	36678779	May Hegglin anomaly	RTPCR
493	4627	MYH9	22	36678779	36678779	May Hegglin anomaly	RTPCR
494	4627	MYH9	22	36678779	36678779	May Hegglin anomaly	RTPCR