List of variants in gene SMCHD1 reported as benign 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: 27

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HGVS	dbSNP	gnomAD frequency
NM_015295.3(SMCHD1):c.4967-15G>T	rs300291	0.98262
NM_015295.3(SMCHD1):c.2122G>A (p.Val708Ile)	rs2276092	0.71166
NM_015295.3(SMCHD1):c.1851A>G (p.Thr617=)	rs635132	0.60549
NM_015295.3(SMCHD1):c.4629C>T (p.Gly1543=)	rs483547	0.39322
NM_015295.3(SMCHD1):c.2637A>T (p.Lys879Asn)	rs633422	0.32971
NM_015295.3(SMCHD1):c.3528A>G (p.Thr1176=)	rs12327477	0.28781
NM_015295.3(SMCHD1):c.4137A>G (p.Ala1379=)	rs2304859	0.28776
NM_015295.3(SMCHD1):c.5476+10A>G	rs3213926	0.28248
NM_015295.3(SMCHD1):c.399T>C (p.Tyr133=)	rs7239096	0.03555
NM_015295.3(SMCHD1):c.2878A>G (p.Ile960Val)	rs9961682	0.03402
NM_015295.3(SMCHD1):c.3612A>T (p.Ser1204=)	rs115632137	0.03072
NM_015295.3(SMCHD1):c.3802-16T>G	rs79829175	0.01859
NM_015295.3(SMCHD1):c.873+7T>C	rs114242799	0.00957
NM_015295.3(SMCHD1):c.1689G>A (p.Leu563=)	rs78073508	0.00657
NM_015295.3(SMCHD1):c.2147-7C>T	rs113524119	0.00473
NM_015295.3(SMCHD1):c.*7A>G	rs140650738	0.00458
NM_015295.3(SMCHD1):c.1419A>G (p.Glu473=)	rs117771893	0.00426
NM_015295.3(SMCHD1):c.4808C>T (p.Thr1603Ile)	rs147034750	0.00303
NM_015295.3(SMCHD1):c.424+10C>T	rs201631086	0.00225
NM_015295.3(SMCHD1):c.1956+7C>T	rs145755468	0.00201
NM_015295.3(SMCHD1):c.4104C>T (p.Pro1368=)	rs117794949	0.00181
NM_015295.3(SMCHD1):c.2913+6C>G	rs186678728	0.00153
NM_015295.3(SMCHD1):c.306G>A (p.Ser102=)	rs7229488	0.00063
NM_015295.3(SMCHD1):c.2147-5C>T	rs184984483	0.00008
NM_015295.3(SMCHD1):c.321A>G (p.Leu107=)	rs567120742	0.00004
NM_015295.3(SMCHD1):c.3519A>G (p.Ile1173Met)	rs536643888	0.00001
NM_015295.3(SMCHD1):c.4847-6del	rs763328487

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