ClinVar Miner

List of variants in gene CIT reported by Undiagnosed Diseases Network, NIH

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_001206999.2(CIT):c.3491A>G (p.Asn1164Ser)	rs145731510	0.00151
NM_001206999.2(CIT):c.652G>A (p.Val218Met)	rs777293258	0.00001

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