List of variants in gene SPINK5 reported as likely benign for not specified

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: 12

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HGVS	dbSNP	gnomAD frequency
NM_006846.4(SPINK5):c.1128C>T (p.Asn376=)	rs78128189	0.00360
NM_006846.4(SPINK5):c.3183G>A (p.Pro1061=)	rs77756935	0.00345
NM_006846.4(SPINK5):c.2442-16A>G	rs148657069	0.00338
NM_006846.4(SPINK5):c.2061G>A (p.Gln687=)	rs36111383	0.00336
NM_006846.4(SPINK5):c.1302+16C>T	rs112708641	0.00241
NM_006846.4(SPINK5):c.2124T>C (p.Ala708=)	rs200884153	0.00058
NM_006846.4(SPINK5):c.803G>A (p.Arg268His)	rs375727921	0.00035
NM_006846.4(SPINK5):c.1539G>A (p.Glu513=)	rs184512279	0.00019
NM_006846.4(SPINK5):c.3189C>T (p.Asp1063=)	rs200751535	0.00018
NM_006846.4(SPINK5):c.1431-13C>T	rs375240260	0.00005
NM_006846.4(SPINK5):c.2667-16T>G	rs1057521635
NM_006846.4(SPINK5):c.81+19G>A	rs1057520976

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