"Genome Diagnostics Laboratory, University Medical Center Utrecht"[sub - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 137396	NM_003923.3(FOXH1):c.771C>T (p.Gly257=)	FOXH1	Single nucleotide variant (synonymous variant)	Holoprosencephaly sequence +2 more	GBenign
Select item 1285043	NM_003923.3(FOXH1):c.410G>C (p.Arg137Pro)	FOXH1 (R137P)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 94385	NM_003923.3(FOXH1):c.338G>C (p.Ser113Thr)	FOXH1 (S113T)	Single nucleotide variant (missense variant)	Holoprosencephaly sequence +2 more	GBenign/Likely benign

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ClinVar