ClinVar Miner

List of variants in gene combination GFAP, LOC130060994 reported as likely benign

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)
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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_002055.5(GFAP):c.1127+10C>A	rs760230360	0.00004
NM_002055.5(GFAP):c.1071G>A (p.Leu357=)	rs1597857653

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