ClinVar Miner

List of variants in gene CYP27B1 studied for multiple sclerosis, susceptibility to 1

Included ClinVar conditions (2):

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_000785.4(CYP27B1):c.1357C>T (p.Arg453Cys)	rs767480544	0.00001
NM_000785.4(CYP27B1):c.1052T>C (p.Leu351Pro)
NM_000785.4(CYP27B1):c.1286G>C (p.Arg429Pro)	rs568165874

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