List of variants in gene TJP2 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: 25

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HGVS	dbSNP	gnomAD frequency
NM_004817.4(TJP2):c.-26G>A	rs147729271	0.00504
NM_004817.4(TJP2):c.2992-8C>T	rs143965233	0.00327
NM_004817.4(TJP2):c.698G>A (p.Arg233Gln)	rs150883816	0.00211
NM_004817.4(TJP2):c.2691C>T (p.Pro897=)	rs149969431	0.00180
NM_004817.4(TJP2):c.185C>T (p.Thr62Met)	rs138241615	0.00168
NM_004817.4(TJP2):c.61-6A>T	rs200415824	0.00145
NM_004817.4(TJP2):c.1877C>G (p.Thr626Ser)	rs149911553	0.00110
NM_004817.4(TJP2):c.1057-17A>G	rs41277895	0.00093
NM_004817.4(TJP2):c.2720T>C (p.Met907Thr)	rs149659876	0.00044
NM_004817.4(TJP2):c.2880+19C>T	rs200384355	0.00044
NM_004817.4(TJP2):c.918C>T (p.Ile306=)	rs374523970	0.00041
NM_004817.4(TJP2):c.3190G>T (p.Val1064Leu)	rs199892018	0.00024
NM_004817.4(TJP2):c.3407+7G>A	rs369322645	0.00015
NM_004817.4(TJP2):c.887G>A (p.Ser296Asn)	rs376434139	0.00014
NM_004817.4(TJP2):c.3063C>T (p.Ala1021=)	rs367977493	0.00013
NM_004817.4(TJP2):c.2880+72G>A	rs397516632	0.00010
NM_004817.4(TJP2):c.2859G>T (p.Ser953=)	rs369972534	0.00009
NM_004817.4(TJP2):c.2970A>G (p.Ala990=)	rs727503481	0.00008
NM_004817.4(TJP2):c.3407+3A>G	rs727505291	0.00007
NM_004817.4(TJP2):c.3225C>T (p.Pro1075=)	rs146241989	0.00005
NM_004817.4(TJP2):c.3372G>A (p.Thr1124=)	rs745427593	0.00001
NM_004817.4(TJP2):c.1521-7A>C	rs373242928
NM_004817.4(TJP2):c.239+14del	rs764370644
NM_004817.4(TJP2):c.2819C>T (p.Pro940Leu)	rs199852211
NM_004817.4(TJP2):c.2865G>A (p.Pro955=)	rs727503480

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