List of variants in gene BMPR1A reported as uncertain significance by PreventionGenetics, part of Exact Sciences

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: 14

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HGVS	dbSNP	gnomAD frequency
NM_004329.3(BMPR1A):c.1235T>C (p.Val412Ala)	rs576247658	0.00014
NM_004329.3(BMPR1A):c.98C>G (p.Thr33Ser)	rs142454490	0.00011
NM_004329.3(BMPR1A):c.478A>G (p.Met160Val)	rs145101532	0.00007
NM_004329.3(BMPR1A):c.760C>T (p.Arg254Cys)	rs587782578	0.00004
NM_004329.3(BMPR1A):c.1596C>G (p.Ile532Met)	rs201345248	0.00003
NM_004329.3(BMPR1A):c.27A>G (p.Arg9=)	rs751420248	0.00002
NM_004329.3(BMPR1A):c.1411C>T (p.Arg471Cys)	rs771452619	0.00001
NM_004329.3(BMPR1A):c.562C>T (p.Arg188Cys)	rs879254272	0.00001
NM_004329.3(BMPR1A):c.101G>C (p.Gly34Ala)	rs730881430
NM_004329.3(BMPR1A):c.1217G>A (p.Arg406His)	rs587780107
NM_004329.3(BMPR1A):c.49A>C (p.Ile17Leu)	rs778886055
NM_004329.3(BMPR1A):c.705G>C (p.Gln235His)	rs780907902
NM_004329.3(BMPR1A):c.712C>G (p.Arg238Gly)	rs747728399
NM_004329.3(BMPR1A):c.785T>C (p.Val262Ala)	rs770830310

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