List of variants in gene SRGAP1 reported as pathogenic for adenocarcinoma

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: 2

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HGVS	dbSNP	gnomAD frequency
NM_020762.4(SRGAP1):c.447A>C (p.Gln149His)	rs781626187	0.00001
NM_020762.4(SRGAP1):c.823G>A (p.Ala275Thr)	rs797044990

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