List of variants in gene IVD reported as likely benign by GeneDx

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: 34

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HGVS	dbSNP	gnomAD frequency
NM_002225.5(IVD):c.1138+78G>A	rs78717580	0.01250
NM_002225.5(IVD):c.456+127A>C	rs113720703	0.01111
NM_002225.5(IVD):c.1066-34G>A	rs113309937	0.01023
NM_002225.5(IVD):c.235-68T>C	rs76137091	0.01002
NM_002225.5(IVD):c.145-110G>A	rs80175544	0.00999
NC_000015.10:g.40405451T>C	rs77818281	0.00975
NC_000015.10:g.40405541T>G	rs137951325	0.00410
NM_002225.5(IVD):c.551-18C>T	rs142064071	0.00363
NM_002225.5(IVD):c.235-19T>C	rs144063157	0.00186
NM_002225.5(IVD):c.11C>T (p.Ala4Val)	rs148189323	0.00157
NM_002225.5(IVD):c.*15G>A	rs112765023	0.00136
NM_002225.5(IVD):c.891G>A (p.Ala297=)	rs138427412	0.00069
NM_002225.5(IVD):c.229C>T (p.Leu77=)	rs143807229	0.00032
NM_002225.5(IVD):c.400A>G (p.Ile134Val)	rs151118565	0.00026
NM_002225.5(IVD):c.234+16C>T	rs750473075	0.00025
NM_002225.5(IVD):c.879-5G>A	rs750569823	0.00014
NM_002225.5(IVD):c.961T>C (p.Leu321=)	rs146011049	0.00011
NM_002225.5(IVD):c.784+13G>A	rs369694967	0.00006
NM_002225.5(IVD):c.1122C>T (p.Asp374=)	rs372504234	0.00005
NM_002225.5(IVD):c.1066-10C>T	rs774472099	0.00003
NM_002225.5(IVD):c.1139-8G>C	rs755640305	0.00003
NM_002225.5(IVD):c.264C>T (p.Gly88=)	rs377199313	0.00003
NM_002225.3(IVD):c.-27C>T	rs545229523	0.00001
NM_002225.5(IVD):c.123G>C (p.Gly41=)	rs139179135	0.00001
NM_002225.5(IVD):c.150T>A (p.Arg50=)	rs762440985	0.00001
NM_002225.5(IVD):c.690T>C (p.Gly230=)	rs1182189552	0.00001
NM_002225.5(IVD):c.784+12C>T	rs572858305	0.00001
NM_002225.5(IVD):c.948C>T (p.Ile316=)	rs754100750	0.00001
NM_002225.5(IVD):c.144+26CCCCAAGGCCTCCTTCCTGCCTGGT[3]	rs373206450
NM_002225.5(IVD):c.234+17G>A	rs568900608
NM_002225.5(IVD):c.286+16_286+17del	rs775497134
NM_002225.5(IVD):c.287-205C>T
NM_002225.5(IVD):c.457-216T>A	rs73383142
NM_002225.5(IVD):c.687+123G>T	rs73383148

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