ClinVar Miner

List of variants in gene ACVR2B reported as benign by Preventiongenetics, part of Exact Sciences

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Gene type:
ClinVar version:
Total variants: 8
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HGVS dbSNP gnomAD frequency
NM_001106.4(ACVR2B):c.333A>G (p.Glu111=) rs2070489 0.51926
NM_001106.4(ACVR2B):c.811-13T>C rs13097628 0.42596
NM_001106.4(ACVR2B):c.1458C>T (p.Asn486=) rs1046048 0.42251
NM_001106.4(ACVR2B):c.1344+7G>T rs9876823 0.01406
NM_001106.4(ACVR2B):c.993C>T (p.Ser331=) rs2228012 0.00761
NM_001106.4(ACVR2B):c.666+5G>A rs187763364 0.00760
NM_001106.4(ACVR2B):c.1075-5C>T rs115155428 0.00657
NM_001106.4(ACVR2B):c.811-12G>A rs144849143 0.00302

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