List of variants in gene RIN2 reported as 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: 9

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HGVS	dbSNP	gnomAD frequency
NM_018993.4(RIN2):c.1818C>T (p.His606=)	rs2076584	0.35224
NM_018993.4(RIN2):c.589T>A (p.Ser197Thr)	rs3803981	0.15165
NM_018993.4(RIN2):c.2001G>A (p.Pro667=)	rs35151304	0.06850
NM_018993.4(RIN2):c.212G>A (p.Cys71Tyr)	rs142502440	0.03307
NM_018993.4(RIN2):c.-11C>T	rs56311184	0.02573
NM_018993.4(RIN2):c.375C>T (p.Thr125=)	rs45481396	0.02341
NM_018993.4(RIN2):c.1044G>C (p.Leu348=)	rs149398614	0.02129
NM_018993.4(RIN2):c.85G>A (p.Gly29Arg)	rs78648341	0.01238
NM_018993.4(RIN2):c.1642G>A (p.Val548Met)	rs181298473

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