List of variants in gene CNNM2 reported as likely benign for disorder of metabolite absorption and transport

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: 16

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HGVS	dbSNP	gnomAD frequency
NM_017649.5(CNNM2):c.360C>T (p.Phe120=)	rs142276906	0.00157
NM_017649.5(CNNM2):c.2073+14T>C	rs184406418	0.00150
NM_017649.5(CNNM2):c.2233+17C>T	rs201729946	0.00091
NM_017649.5(CNNM2):c.903C>T (p.Tyr301=)	rs140279763	0.00044
NM_017649.5(CNNM2):c.604G>A (p.Ala202Thr)	rs75800852	0.00034
NM_017649.5(CNNM2):c.342G>T (p.Thr114=)	rs375416482	0.00029
NM_017649.5(CNNM2):c.804G>T (p.Leu268=)	rs148386496	0.00013
NM_017649.5(CNNM2):c.2565C>T (p.Asn855=)	rs540196504	0.00003
NM_017649.5(CNNM2):c.621C>T (p.Ser207=)	rs767302259	0.00002
NM_017649.5(CNNM2):c.1765+11T>C	rs901937775	0.00001
NM_017649.5(CNNM2):c.2073+8G>T	rs1302420255	0.00001
NM_017649.5(CNNM2):c.2322A>G (p.Thr774=)	rs756002318	0.00001
NM_017649.5(CNNM2):c.2240A>G (p.Asn747Ser)	rs988049940
NM_017649.5(CNNM2):c.551A>G (p.Glu184Gly)
NM_017649.5(CNNM2):c.557G>C (p.Ser186Thr)
NM_017649.5(CNNM2):c.778A>T (p.Ile260Phe)

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