List of variants in gene GRHL3 reported as likely benign for Van der Woude syndrome 2

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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: 15

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HGVS	dbSNP	gnomAD frequency
NM_198173.3(GRHL3):c.1159C>T (p.Arg387Cys)	rs147284380	0.00093
NM_198173.3(GRHL3):c.614C>T (p.Ser205Leu)	rs201073516	0.00036
NM_198173.3(GRHL3):c.672C>T (p.Tyr224=)	rs779916210	0.00001
NM_198173.3(GRHL3):c.117G>A (p.Pro39=)
NM_198173.3(GRHL3):c.1227C>T (p.Arg409=)
NM_198173.3(GRHL3):c.1287C>T (p.Gly429=)
NM_198173.3(GRHL3):c.1419+10G>A	rs2148660639
NM_198173.3(GRHL3):c.1531G>A (p.Asp511Asn)
NM_198173.3(GRHL3):c.1534C>T (p.Leu512Phe)
NM_198173.3(GRHL3):c.17+13C>G
NM_198173.3(GRHL3):c.318C>T (p.Pro106=)
NM_198173.3(GRHL3):c.348C>T (p.Asn116=)
NM_198173.3(GRHL3):c.686+11C>A
NM_198173.3(GRHL3):c.686+18G>C
NM_198173.3(GRHL3):c.933G>A (p.Lys311=)

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