List of variants in gene GP1BA reported as likely 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: 8

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HGVS	dbSNP	gnomAD frequency
NM_000173.7(GP1BA):c.106A>G (p.Arg36Gly)	rs111292798	0.00526
NM_000173.7(GP1BA):c.732C>T (p.Tyr244=)	rs200381725	0.00102
NM_000173.7(GP1BA):c.1173C>T (p.Pro391=)	rs369052917	0.00004
NM_000173.7(GP1BA):c.1224G>T (p.Pro408=)
NM_000173.7(GP1BA):c.1233A>G (p.Pro411=)
NM_000173.7(GP1BA):c.1452C>T (p.Pro484=)
NM_000173.7(GP1BA):c.321C>T (p.Ser107=)
NM_000173.7(GP1BA):c.390G>A (p.Ser130=)

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