List of variants in gene RHOBTB2 reported as benign by CeGaT Center for Human Genetics Tuebingen

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: 10

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HGVS	dbSNP	gnomAD frequency
NM_015178.3(RHOBTB2):c.438C>T (p.Tyr146=)	rs139953909	0.00968
NM_015178.3(RHOBTB2):c.168C>T (p.Ile56=)	rs61732770	0.00331
NM_015178.3(RHOBTB2):c.1931G>A (p.Arg644His)	rs117851304	0.00247
NM_015178.3(RHOBTB2):c.734T>C (p.Val245Ala)	rs146491810	0.00144
NM_015178.3(RHOBTB2):c.2129C>T (p.Pro710Leu)	rs146723409	0.00064
NM_015178.3(RHOBTB2):c.1180G>A (p.Val394Met)	rs146017675	0.00024
NM_015178.3(RHOBTB2):c.1640G>A (p.Ser547Asn)	rs202072436	0.00007
NM_001160036.2(RHOBTB2):c.-23-3C>T
NM_015178.3(RHOBTB2):c.-122T>G
NM_015178.3(RHOBTB2):c.-438C>G

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