List of variants in gene TPM2 reported as benign for arthrogryposis syndrome

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: 21

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HGVS	dbSNP	gnomAD frequency
NM_213674.1(TPM2):c.-137T>A	rs3793540	0.23673
NM_213674.1(TPM2):c.-136T>A	rs3793539	0.23669
NM_213674.1(TPM2):c.-135T>A	rs3793538	0.23661
NM_003289.4(TPM2):c.*8G>A	rs56249943	0.06243
NM_003289.4(TPM2):c.773-4_773-3insA	rs1554658501	0.02101
NM_003289.4(TPM2):c.564-18dup	rs776086128	0.00099
NM_003289.4(TPM2):c.563+17G>A	rs201633747	0.00062
NM_003289.4(TPM2):c.726C>T (p.Ala242=)	rs76414035	0.00045
NM_003289.4(TPM2):c.-65C>T	rs377242459	0.00003
NM_003289.4(TPM2):c.563+18T>A	rs370352040	0.00001
NM_003289.4(TPM2):c.*7C>T	rs79882576
NM_003289.4(TPM2):c.300C>T (p.Asp100=)	rs532190742
NM_003289.4(TPM2):c.375-12C>A
NM_003289.4(TPM2):c.564-19del	rs3215700
NM_003289.4(TPM2):c.564-19dup	rs3215700
NM_003289.4(TPM2):c.564-20_564-19dup	rs3215700
NM_003289.4(TPM2):c.564-6dup	rs1439651784
NM_003289.4(TPM2):c.773-3del	rs35401252
NM_003289.4(TPM2):c.773-3dup	rs35401252
NM_003289.4(TPM2):c.773-4_773-3dup	rs35401252
NM_003289.4(TPM2):c.773-5_773-3dup	rs35401252

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