List of variants in gene combination ABCA12, SNHG31 reported by Fulgent Genetics, Fulgent Genetics

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 6

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HGVS	dbSNP	gnomAD frequency
NM_173076.3(ABCA12):c.7093G>A (p.Asp2365Asn)	rs726070	0.02279
NM_173076.3(ABCA12):c.7715A>G (p.Tyr2572Cys)	rs199846944	0.00019
NM_173076.3(ABCA12):c.6785_6852+13delinsT
NM_173076.3(ABCA12):c.6858del (p.Phe2286fs)	rs751949857
NM_173076.3(ABCA12):c.6963-1G>A
NM_173076.3(ABCA12):c.7323del (p.Val2442fs)	rs387906284

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