ClinVar Miner

List of variants in gene SRGAP1 reported as uncertain significance for congenital anomalies of kidney and urinary tract 1

Included ClinVar conditions (1):

Congenital anomalies of kidney and urinary tract 1

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_020762.4(SRGAP1):c.1993C>A (p.Pro665Thr)	rs1592332125

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