List of variants in gene combination CENPP, OMD reported as uncertain significance 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: 30

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HGVS	dbSNP	gnomAD frequency
NM_005014.3(OMD):c.1102A>G (p.Thr368Ala)	rs35709442	0.00094
NM_005014.3(OMD):c.737C>A (p.Ser246Tyr)	rs149148413	0.00016
NM_005014.3(OMD):c.1073A>G (p.His358Arg)	rs142056236	0.00013
NM_005014.3(OMD):c.1007G>A (p.Arg336His)	rs372233789	0.00007
NM_005014.3(OMD):c.719T>C (p.Leu240Ser)	rs1245481818	0.00005
NM_005014.3(OMD):c.850G>C (p.Glu284Gln)	rs376470384	0.00005
NM_005014.3(OMD):c.827T>C (p.Ile276Thr)	rs369950897	0.00004
NM_005014.3(OMD):c.1228G>A (p.Gly410Arg)	rs189375297	0.00003
NM_005014.3(OMD):c.269C>T (p.Pro90Leu)	rs142713990	0.00003
NM_005014.3(OMD):c.214T>C (p.Phe72Leu)	rs374973890	0.00002
NM_005014.3(OMD):c.1057T>A (p.Cys353Ser)	rs147807372	0.00001
NM_005014.3(OMD):c.1072C>T (p.His358Tyr)	rs1390215556	0.00001
NM_005014.3(OMD):c.1097G>A (p.Arg366Gln)	rs1207692640	0.00001
NM_005014.3(OMD):c.286C>T (p.Leu96Phe)	rs1381601912	0.00001
NM_005014.3(OMD):c.602C>T (p.Ser201Phe)	rs776124805	0.00001
NM_005014.3(OMD):c.1068T>A (p.His356Gln)	rs1843559768
NM_005014.3(OMD):c.1088G>A (p.Gly363Asp)
NM_005014.3(OMD):c.1106A>C (p.Asn369Thr)
NM_005014.3(OMD):c.1118T>C (p.Ile373Thr)
NM_005014.3(OMD):c.1180G>A (p.Asp394Asn)
NM_005014.3(OMD):c.1206C>A (p.Ser402Arg)
NM_005014.3(OMD):c.146T>C (p.Val49Ala)
NM_005014.3(OMD):c.202T>C (p.Cys68Arg)
NM_005014.3(OMD):c.395T>C (p.Ile132Thr)	rs1843639189
NM_005014.3(OMD):c.515A>G (p.Asn172Ser)
NM_005014.3(OMD):c.571C>T (p.Leu191Phe)	rs1843633813
NM_005014.3(OMD):c.679A>G (p.Met227Val)
NM_005014.3(OMD):c.707T>G (p.Met236Arg)	rs781234688
NM_005014.3(OMD):c.779A>G (p.His260Arg)
NM_005014.3(OMD):c.844A>G (p.Ile282Val)	rs2491735133

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