ClinVar Miner

List of variants in gene combination FOXH1, KIFC2 reported as likely benign for Holoprosencephaly sequence

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Total variants: 3
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HGVS dbSNP
NM_003923.3(FOXH1):c.*311C>T rs74360910
NM_003923.3(FOXH1):c.*472G>T rs576710211
NM_003923.3(FOXH1):c.*55C>T rs192907579

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