ClinVar Miner

List of variants in gene RUNX2 reported as likely pathogenic for not provided

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Total variants: 25
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HGVS dbSNP gnomAD frequency
NM_001024630.4(RUNX2):c.1088-1G>A rs2150453696
NM_001024630.4(RUNX2):c.1088-2A>C rs2150453692
NM_001024630.4(RUNX2):c.1379dup (p.Asp463fs) rs1582232661
NM_001024630.4(RUNX2):c.354C>A (p.Ser118Arg)
NM_001024630.4(RUNX2):c.391C>G (p.Arg131Gly)
NM_001024630.4(RUNX2):c.401A>C (p.Lys134Thr)
NM_001024630.4(RUNX2):c.424-2A>G rs2150368149
NM_001024630.4(RUNX2):c.436G>A (p.Gly146Arg)
NM_001024630.4(RUNX2):c.467T>A (p.Val156Asp)
NM_001024630.4(RUNX2):c.480C>G (p.Asn160Lys)
NM_001024630.4(RUNX2):c.495del (p.Ala166fs)
NM_001024630.4(RUNX2):c.505C>T (p.Arg169Trp) rs1203066173
NM_001024630.4(RUNX2):c.572G>A (p.Ser191Asn) rs104893990
NM_001024630.4(RUNX2):c.581-2A>C
NM_001024630.4(RUNX2):c.581-2del
NM_001024630.4(RUNX2):c.59-2A>G
NM_001024630.4(RUNX2):c.597G>T (p.Leu199Phe) rs2150371841
NM_001024630.4(RUNX2):c.650T>G (p.Ile217Ser) rs2150371895
NM_001024630.4(RUNX2):c.664G>C (p.Asp222His) rs1798736907
NM_001024630.4(RUNX2):c.665A>G (p.Asp222Gly) rs2150371921
NM_001024630.4(RUNX2):c.685+1G>C
NM_001024630.4(RUNX2):c.686-1G>A rs2150407530
NM_001024630.4(RUNX2):c.686-2A>G
NM_001024630.4(RUNX2):c.860-1G>A
NM_001024630.4(RUNX2):c.860-1G>T rs2150421181

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