List of variants in gene SLC37A4 reported as likely 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: 13

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HGVS	dbSNP	gnomAD frequency
NM_001164277.2(SLC37A4):c.593A>T (p.Asn198Ile)	rs34203644	0.00280
NM_001164277.2(SLC37A4):c.540C>T (p.Ser180=)	rs371716153	0.00262
NM_001164277.2(SLC37A4):c.-700+9C>T	rs534659292	0.00077
NM_001164277.2(SLC37A4):c.785+6A>T	rs369358436	0.00072
NM_001164277.2(SLC37A4):c.-700+10G>T	rs1057522895	0.00006
NM_001164277.2(SLC37A4):c.-183C>T	rs145369754	0.00004
NM_001164277.2(SLC37A4):c.381+15A>G	rs1057520372	0.00003
NM_001164277.2(SLC37A4):c.1098C>T (p.His366=)	rs782587864	0.00002
NM_001164277.2(SLC37A4):c.786-7A>G	rs781887799	0.00001
NM_001164277.2(SLC37A4):c.*11G>A	rs978301169
NM_001164277.2(SLC37A4):c.-196+14C>T	rs1555192097
NM_001164277.2(SLC37A4):c.1067G>C (p.Ser356Thr)	rs547488738
NM_001164277.2(SLC37A4):c.492C>T (p.Ser164=)	rs369399624

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