List of variants in gene PAFAH1B1 reported by Ambry 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: 9

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HGVS	dbSNP	gnomAD frequency
NM_000430.4(PAFAH1B1):c.608A>G (p.Asn203Ser)	rs377583144	0.00013
NM_000430.4(PAFAH1B1):c.958A>G (p.Ile320Val)	rs144659773	0.00013
NM_000430.4(PAFAH1B1):c.566A>C (p.His189Pro)	rs1030536153	0.00001
NM_000430.4(PAFAH1B1):c.650A>T (p.Lys217Ile)	rs1305223107	0.00001
NM_000430.4(PAFAH1B1):c.163T>A (p.Trp55Arg)	rs587784254
NM_000430.4(PAFAH1B1):c.416C>G (p.Thr139Ser)	rs2544096699
NM_000430.4(PAFAH1B1):c.569-10T>C	rs113994202
NM_000430.4(PAFAH1B1):c.703_704del (p.Glu235fs)	rs797045865
NM_000430.4(PAFAH1B1):c.994A>G (p.Met332Val)	rs2069271632

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