ClinVar Miner

List of variants in gene GLA, HNRNPH2, RPL36A-HNRNPH2 studied for Fabry disease

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
NC_000023.11:g.101408672C>G	rs3027580	0.06337
NM_000169.3(GLA):c.335G>A (p.Arg112His)	rs372966991	0.00002
NC_000023.11:g.101408476G>C	rs782312723

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