List of variants reported as not provided for Rahman syndrome by GeneReviews

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Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 17

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HGVS	dbSNP	gnomAD frequency
NM_005321.3(H1-4):c.365dup (p.Ala123fs)	rs768525914
NM_005321.3(H1-4):c.406_407insT (p.Lys136fs)	rs1764192704
NM_005321.3(H1-4):c.407dup (p.Lys137fs)	rs1764192628
NM_005321.3(H1-4):c.408dup (p.Lys137fs)	rs1581429395
NM_005321.3(H1-4):c.414dup (p.Lys139fs)	rs1581429403
NM_005321.3(H1-4):c.416dup (p.Lys140fs)	rs1764193257
NM_005321.3(H1-4):c.425_431delinsAGGGGGTT (p.Thr142fs)	rs1581429434
NM_005321.3(H1-4):c.425delinsAG (p.Thr142fs)	rs1581429431
NM_005321.3(H1-4):c.430dup (p.Ala144fs)	rs1131690805
NM_005321.3(H1-4):c.431dup (p.Ala145fs)	rs1764194450
NM_005321.3(H1-4):c.433dup (p.Ala145fs)	rs1554162872
NM_005321.3(H1-4):c.435dup (p.Thr146fs)	rs1764194669
NM_005321.3(H1-4):c.436_458del (p.Thr146fs)	rs1131690807
NM_005321.3(H1-4):c.440_441del (p.Pro147fs)	rs1131690806
NM_005321.3(H1-4):c.447dup (p.Ser150fs)	rs1581429514
NM_005321.3(H1-4):c.454_455insT (p.Lys152fs)	rs1554162894
NM_005321.3(H1-4):c.464dup (p.Lys157fs)	rs1581429554

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