List of variants in gene ABHD12 reported as likely benign by CeGaT Center for Human Genetics Tuebingen

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: 8

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HGVS	dbSNP	gnomAD frequency
NM_001042472.3(ABHD12):c.1041C>T (p.Ile347=)	rs188888939	0.00036
NM_001042472.3(ABHD12):c.960C>T (p.His320=)	rs146195280	0.00023
NM_001042472.3(ABHD12):c.1044C>T (p.Ala348=)	rs371418239	0.00020
NM_001042472.3(ABHD12):c.453C>T (p.Asn151=)	rs375299452	0.00009
NM_001042472.3(ABHD12):c.375G>A (p.Thr125=)	rs1048930924	0.00001
NM_001042472.3(ABHD12):c.162C>G (p.Ala54=)	rs1445435596
NM_001042472.3(ABHD12):c.183G>T (p.Ala61=)	rs2146161198
NM_001042472.3(ABHD12):c.783G>A (p.Glu261=)

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