List of variants in gene BMPR1A reported as 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_004329.3(BMPR1A):c.4C>A (p.Pro2Thr)	rs11528010	0.40719
NM_004329.3(BMPR1A):c.1343-11T>C	rs7074064	0.40534
NM_004329.3(BMPR1A):c.431-26T>A	rs7920259	0.06507
NM_004329.3(BMPR1A):c.435G>A (p.Pro145=)	rs11818239	0.04296
NM_004329.3(BMPR1A):c.675+12G>A	rs12267107	0.04183
NM_004329.3(BMPR1A):c.1342+6A>G	rs55763614	0.02404
NM_004329.3(BMPR1A):c.67+46C>T	rs73351703	0.01806
NM_004329.3(BMPR1A):c.1140C>T (p.Asp380=)	rs35572415	0.01512
NM_004329.3(BMPR1A):c.-25A>G	rs116346662	0.01322
NM_004329.3(BMPR1A):c.618A>G (p.Leu206=)	rs55992440	0.00257
NM_004329.3(BMPR1A):c.777G>A (p.Ala259=)	rs56108371	0.00192
NM_004329.3(BMPR1A):c.1299C>T (p.Phe433=)	rs150946485	0.00153
NM_004329.3(BMPR1A):c.1560G>A (p.Thr520=)	rs142775086	0.00136
NM_004329.3(BMPR1A):c.1395G>C (p.Pro465=)	rs55845713	0.00089
NM_004329.3(BMPR1A):c.1419T>G (p.Val473=)	rs145756629	0.00058
NM_004329.3(BMPR1A):c.676-6A>C	rs186999445	0.00014
NM_004329.3(BMPR1A):c.961C>T (p.Leu321=)	rs377412651	0.00011
NM_004329.3(BMPR1A):c.530+13T>G	rs367550999	0.00010
NM_004329.3(BMPR1A):c.33G>A (p.Leu11=)	rs535411352	0.00009
NM_004329.3(BMPR1A):c.1474-10T>C	rs369633360	0.00004
NM_004329.3(BMPR1A):c.1536C>T (p.Leu512=)	rs758796892	0.00001
NM_004329.3(BMPR1A):c.230+37G>A	rs201927554	0.00001
NM_004329.3(BMPR1A):c.682C>A (p.Arg228=)	rs587782682	0.00001
NM_004329.3(BMPR1A):c.1395G>A (p.Pro465=)	rs55845713
NM_004329.3(BMPR1A):c.231-10dup	rs747206781

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