List of variants in gene TMEM216 reported as 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: 10

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HGVS	dbSNP	gnomAD frequency
NM_001173990.2(TMEM216):c.-443T>C	rs10750955	0.84580
NM_001173990.3(TMEM216):c.264G>A (p.Pro88=)	rs3741265	0.84043
NM_001173990.3(TMEM216):c.432-11_432-10insA	rs11382548	0.83974
NM_001173990.3(TMEM216):c.432-1G>C	rs10897158	0.83918
NM_001173990.3(TMEM216):c.-2G>T	rs7107543	0.08005
NM_001173990.3(TMEM216):c.229+78A>G	rs11827662	0.06115
NM_001173990.3(TMEM216):c.432-33A>G	rs114624627	0.03226
NM_001173990.3(TMEM216):c.*444T>C	rs116047887	0.02086
NM_001173990.3(TMEM216):c.35-17C>T	rs147953784	0.00450
NM_001173990.3(TMEM216):c.-24C>G	rs59493015

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