List of variants in gene combination CCDST, FLG2 reported as likely benign for not specified

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: 19

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HGVS	dbSNP	gnomAD frequency
NM_001014342.3(FLG2):c.311G>A (p.Arg104His)	rs140914817	0.00050
NM_001014342.3(FLG2):c.1208G>A (p.Arg403His)	rs149294520	0.00014
NM_001014342.3(FLG2):c.4923A>T (p.Arg1641Ser)	rs756082008	0.00006
NM_001014342.3(FLG2):c.5983G>A (p.Gly1995Arg)	rs148224294	0.00002
NM_001014342.3(FLG2):c.6679G>A (p.Gly2227Arg)	rs1232071067	0.00001
NM_001014342.3(FLG2):c.1335T>G (p.His445Gln)
NM_001014342.3(FLG2):c.2837T>C (p.Phe946Ser)	rs746313861
NM_001014342.3(FLG2):c.3215G>A (p.Arg1072His)	rs767452601
NM_001014342.3(FLG2):c.3566T>C (p.Phe1189Ser)
NM_001014342.3(FLG2):c.3923G>A (p.Arg1308His)	rs201967124
NM_001014342.3(FLG2):c.4164T>A (p.His1388Gln)	rs756210248
NM_001014342.3(FLG2):c.4261G>A (p.Gly1421Arg)
NM_001014342.3(FLG2):c.4784G>A (p.Arg1595Gln)
NM_001014342.3(FLG2):c.5703C>G (p.His1901Gln)
NM_001014342.3(FLG2):c.5888G>T (p.Gly1963Val)
NM_001014342.3(FLG2):c.6098A>C (p.Tyr2033Ser)	rs755816906
NM_001014342.3(FLG2):c.6132C>A (p.His2044Gln)
NM_001014342.3(FLG2):c.6132C>G (p.His2044Gln)
NM_001014342.3(FLG2):c.6709T>C (p.Tyr2237His)

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