ClinVar Miner

List of variants in gene combination CASQ2, VANGL1 reported as benign for Caudal regression sequence

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Total variants: 13
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HGVS dbSNP
NM_138959.3(VANGL1):c.*4478C>T rs17034226
NM_138959.3(VANGL1):c.*4504C>T rs17034228
NM_138959.3(VANGL1):c.*5266C>T rs17034230
NM_138959.3(VANGL1):c.*5368G>A rs10494179
NM_138959.3(VANGL1):c.*5633T>G rs4348723
NM_138959.3(VANGL1):c.*5751A>G rs10801933
NM_138959.3(VANGL1):c.*5841A>T rs4548441
NM_138959.3(VANGL1):c.*5995A>T rs4595366
NM_138959.3(VANGL1):c.*6026G>A rs6428677
NM_138959.3(VANGL1):c.*6199A>T rs3811007
NM_138959.3(VANGL1):c.*6212C>T rs3811006
NM_138959.3(VANGL1):c.*6321T>G rs77318780
NM_138959.3(VANGL1):c.*6721A>G rs17034249

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