List of variants in gene SLC37A4 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: 30

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HGVS	dbSNP	gnomAD frequency
NM_001164277.1(SLC37A4):c.-755T>A	rs1784559	0.50768
NM_001164277.2(SLC37A4):c.-516G>A	rs3759012	0.44121
NM_001164277.2(SLC37A4):c.*125G>C	rs8301	0.28659
NM_001164277.2(SLC37A4):c.-195-136A>C	rs58412813	0.28510
NM_001164277.2(SLC37A4):c.1224G>A (p.Thr408=)	rs8192696	0.24878
NM_001164277.2(SLC37A4):c.986-76T>C	rs2276072	0.21113
NM_001164277.2(SLC37A4):c.986-77T>G	rs2276071	0.20745
NM_001164277.2(SLC37A4):c.-195-64C>T	rs56258965	0.15980
NM_001164277.2(SLC37A4):c.626+19C>T	rs741811	0.11021
NM_001164277.2(SLC37A4):c.148+215C>T	rs61902084	0.06150
NM_001164277.2(SLC37A4):c.-195-89C>T	rs11217128	0.05282
NM_001164277.2(SLC37A4):c.183T>C (p.Ala61=)	rs34123220	0.04188
NM_001164277.2(SLC37A4):c.-700+31A>C	rs75634142	0.04103
NM_001164277.2(SLC37A4):c.626+76C>T	rs79511838	0.04103
NM_001164277.2(SLC37A4):c.786-74T>C	rs73559193	0.03303
NM_001164277.2(SLC37A4):c.871+50C>T	rs78121950	0.03211
NM_001164277.2(SLC37A4):c.871+51G>A	rs77180649	0.02860
NM_001164277.2(SLC37A4):c.148+174G>A	rs80235222	0.02857
NC_000011.10:g.119030939C>A	rs114116089	0.01997
NM_001164277.2(SLC37A4):c.626+102G>A	rs73559195	0.01903
NM_001164277.2(SLC37A4):c.1278G>A (p.Lys426=)	rs34871377	0.01583
NM_001164277.2(SLC37A4):c.626+14C>T	rs56394886	0.01293
NM_001164277.2(SLC37A4):c.149-14A>G	rs79849261	0.01232
NM_001164277.2(SLC37A4):c.1275C>T (p.Ser425=)	rs35010541	0.01045
NM_001164277.2(SLC37A4):c.1062C>T (p.Asn354=)	rs61730035	0.00758
NM_001164277.2(SLC37A4):c.593A>T (p.Asn198Ile)	rs34203644	0.00280
NM_001164277.2(SLC37A4):c.*17G>A	rs782225728	0.00002
NM_001164277.2(SLC37A4):c.149-82G>A	rs4936459
NM_001164277.2(SLC37A4):c.627-157G>A	rs74888816
NM_001164277.2(SLC37A4):c.872-169C>T	rs57156480

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