List of variants in gene GCM2 reported by Martin Pollak Laboratory, Beth Israel Deaconess Medical Center

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 10

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HGVS	dbSNP	gnomAD frequency
NM_004752.4(GCM2):c.477T>C (p.His159=)	rs387907431	0.00001
NM_004752.4(GCM2):c.1168T>C (p.Ser390Pro)	rs387907434
NM_004752.4(GCM2):c.1277A>C (p.Tyr426Ser)	rs387907433
NM_004752.4(GCM2):c.303G>T (p.Leu101=)	rs387907432
NM_004752.4(GCM2):c.665A>T (p.Glu222Val)	rs387907429
NM_004752.4(GCM2):c.782A>T (p.Tyr261Phe)	rs387907430
NM_004752.4(GCM2):c.831G>T (p.Leu277Phe)	rs369540974
NM_004752.4(GCM2):c.833C>T (p.Ala278Val)	rs387907426
NM_004752.4(GCM2):c.852T>C (p.Asn284=)	rs387907428
NM_004752.4(GCM2):c.906A>T (p.Thr302=)	rs387907427

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