List of variants in gene TMLHE reported as uncertain significance for autism, susceptiblity to

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: 6

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HGVS	dbSNP	gnomAD frequency
NM_018196.4(TMLHE):c.278G>A (p.Arg93His)	rs145371120	0.00016
NM_018196.4(TMLHE):c.491C>T (p.Ser164Leu)	rs369612445	0.00002
NM_018196.4(TMLHE):c.523G>A (p.Glu175Lys)
NM_018196.4(TMLHE):c.638+83_995+2127del
NM_018196.4(TMLHE):c.6G>T (p.Trp2Cys)	rs782121512
NM_018196.4(TMLHE):c.995+2T>C

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