List of variants in gene GRHL2 reported as benign by Laboratory for Molecular Medicine, Mass General Brigham Personalized Medicine

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: 9

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HGVS	dbSNP	gnomAD frequency
NM_024915.4(GRHL2):c.26A>G (p.Lys9Arg)	rs3735709	0.02044
NM_024915.4(GRHL2):c.651C>T (p.Ser217=)	rs34332949	0.01341
NM_024915.4(GRHL2):c.1243G>A (p.Val415Ile)	rs3779617	0.00608
NM_024915.4(GRHL2):c.1500G>A (p.Thr500=)	rs34550163	0.00460
NM_024915.4(GRHL2):c.1517+12A>G	rs142083150	0.00458
NM_024915.4(GRHL2):c.1098+9C>T	rs189993760	0.00370
NM_024915.4(GRHL2):c.*6G>A	rs116154722	0.00228
NM_024915.4(GRHL2):c.1806G>C (p.Ser602=)	rs61732855
NM_024915.4(GRHL2):c.285-14del	rs727504472

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