List of variants in gene GRHL2 reported as uncertain significance 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: 11

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HGVS	dbSNP	gnomAD frequency
NM_024915.4(GRHL2):c.548G>A (p.Arg183Gln)	rs142411476	0.00014
NM_024915.4(GRHL2):c.1690A>T (p.Met564Leu)	rs200592171	0.00012
NM_024915.4(GRHL2):c.641G>A (p.Ser214Asn)	rs199931364	0.00011
NM_024915.4(GRHL2):c.83C>G (p.Ala28Gly)	rs561693958	0.00004
NM_024915.4(GRHL2):c.1081G>A (p.Val361Met)	rs770962467	0.00003
NM_024915.4(GRHL2):c.685C>T (p.Arg229Trp)	rs766515922	0.00002
NM_024915.4(GRHL2):c.1723G>A (p.Val575Met)	rs370196002
NM_024915.4(GRHL2):c.1764-12C>G	rs371424751
NM_024915.4(GRHL2):c.319T>A (p.Leu107Met)	rs1048525846
NM_024915.4(GRHL2):c.449T>G (p.Ile150Ser)	rs727504883
NM_024915.4(GRHL2):c.974A>C (p.His325Pro)	rs1586112160

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