ClinVar Miner

List of variants in gene combination LOC130009809, RNASEH2B reported as benign for Aicardi-Goutieres syndrome 2

Included ClinVar conditions (1):

Aicardi-Goutieres syndrome 2

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 1

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HGVS	dbSNP	gnomAD frequency
NM_024570.4(RNASEH2B):c.-210G>C	rs112702177	0.02962

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