List of variants in gene SLC6A8 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: 14

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HGVS	dbSNP	gnomAD frequency
NM_005629.4(SLC6A8):c.-5A>G	rs384573	1.00000
NM_005629.4(SLC6A8):c.1496-5C>T	rs200695210	0.00491
NM_005629.4(SLC6A8):c.1768-3C>T	rs150207268	0.00435
NM_005629.4(SLC6A8):c.1141+18G>A	rs187400676	0.00362
NM_005629.4(SLC6A8):c.1437C>T (p.Ser479=)	rs140115896	0.00334
NM_005629.4(SLC6A8):c.1496-18C>T	rs201867256	0.00203
NM_005629.4(SLC6A8):c.780C>T (p.Ile260=)	rs148232368	0.00177
NM_005629.4(SLC6A8):c.777+4C>T	rs201581661	0.00063
NM_005629.4(SLC6A8):c.1496-8C>T	rs376038235	0.00038
NM_005629.4(SLC6A8):c.1516G>A (p.Asp506Asn)	rs201526436	0.00036
NM_005629.4(SLC6A8):c.1678A>G (p.Met560Val)	rs145438966	0.00024
NM_005629.4(SLC6A8):c.87G>C (p.Gly29=)	rs782373793	0.00011
NM_005629.4(SLC6A8):c.1870G>A (p.Glu624Lys)	rs368555229	0.00003
NM_005629.4(SLC6A8):c.87G>A (p.Gly29=)	rs782373793

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