List of variants in gene OBSCN reported as likely benign by ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories

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: 13

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HGVS	dbSNP	gnomAD frequency
NM_001386125.1(OBSCN):c.10654G>A (p.Asp3552Asn)	rs201332233	0.00028
NM_001386125.1(OBSCN):c.20021G>A (p.Ser6674Asn)	rs376194851	0.00019
NM_001386125.1(OBSCN):c.2050T>C (p.Phe684Leu)	rs371434948	0.00016
NM_001386125.1(OBSCN):c.3185C>T (p.Ser1062Phe)	rs200058427	0.00013
NM_001386125.1(OBSCN):c.12134C>T (p.Ser4045Leu)	rs779979102	0.00010
NM_001386125.1(OBSCN):c.9499A>G (p.Ile3167Val)	rs764679750	0.00004
NM_001386125.1(OBSCN):c.17133G>A (p.Thr5711=)	rs372921390	0.00003
NM_001386125.1(OBSCN):c.5647G>A (p.Glu1883Lys)	rs371852931	0.00002
NM_001386125.1(OBSCN):c.16314T>G (p.Thr5438=)	rs1558320744	0.00001
NM_001386125.1(OBSCN):c.9172G>A (p.Ala3058Thr)	rs1433965473	0.00001
NM_001386125.1(OBSCN):c.11041G>A (p.Gly3681Arg)	rs200870329
NM_001386125.1(OBSCN):c.15852G>A (p.Thr5284=)	rs370387618
NM_001386125.1(OBSCN):c.17582T>G (p.Phe5861Cys)	rs936285838

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