List of variants in gene PAFAH1B1 reported as likely benign for not specified

Minimum submission review status:		Collection method:
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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 10

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HGVS	dbSNP	gnomAD frequency
NM_000430.4(PAFAH1B1):c.568+27C>T	rs3213696	0.89105
NM_000430.4(PAFAH1B1):c.118-14T>C	rs147692085	0.00468
NM_000430.4(PAFAH1B1):c.780A>G (p.Val260=)	rs150380620	0.00111
NM_000430.4(PAFAH1B1):c.387T>C (p.Asp129=)	rs140936904	0.00055
NM_000430.4(PAFAH1B1):c.1110G>A (p.Lys370=)	rs147983048	0.00021
NM_000430.4(PAFAH1B1):c.958A>G (p.Ile320Val)	rs144659773	0.00013
NM_000430.4(PAFAH1B1):c.1003-11T>C	rs371584771	0.00010
NM_000430.4(PAFAH1B1):c.1002C>T (p.Leu334=)	rs199648962	0.00007
NM_000430.4(PAFAH1B1):c.690C>T (p.Phe230=)	rs1351403324	0.00002
NM_000430.4(PAFAH1B1):c.400-13G>A	rs1346378389	0.00001

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