List of variants in gene TTC21B reported as likely pathogenic for Jeune thoracic dystrophy; Nephronophthisis

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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_024753.5(TTC21B):c.1386+1G>T	rs764514397	0.00002
NM_024753.5(TTC21B):c.1087+1G>A	rs776301212	0.00001
NM_024753.5(TTC21B):c.3102-2A>G	rs779472675	0.00001
NM_024753.5(TTC21B):c.553-2A>G	rs773580610	0.00001
NC_000002.11:g.(?_166767817)_(166806254_?)dup
NM_024753.5(TTC21B):c.1516+1G>A
NM_024753.5(TTC21B):c.1516+2T>G	rs748598334
NM_024753.5(TTC21B):c.152-1G>A	rs371396651
NM_024753.5(TTC21B):c.152-2A>G	rs760214276
NM_024753.5(TTC21B):c.1900-1G>T
NM_024753.5(TTC21B):c.1900-2A>G
NM_024753.5(TTC21B):c.2138+1G>T
NM_024753.5(TTC21B):c.2461+1G>A
NM_024753.5(TTC21B):c.2868+1G>T	rs1685487857
NM_024753.5(TTC21B):c.2869-2A>G	rs1553508246
NM_024753.5(TTC21B):c.3263+1G>A	rs1574070787
NM_024753.5(TTC21B):c.3684+1G>A
NM_024753.5(TTC21B):c.711-2A>C	rs1686972152
NM_024753.5(TTC21B):c.895-1G>A	rs773008707

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