List of variants in gene GP1BA reported as benign by GeneDx

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_000173.7(GP1BA):c.1311A>G (p.Pro437=)	rs2586529	0.65526
NM_000173.7(GP1BA):c.1322_1344del (p.Ser441fs)	rs770089708	0.39537
NM_000173.7(GP1BA):c.-6-42A>T	rs81663	0.26489
NM_000173.7(GP1BA):c.-5T>C	rs2243093	0.17006
NM_000173.7(GP1BA):c.482C>T (p.Thr161Met)	rs6065	0.12253
NM_000173.7(GP1BA):c.1074A>G (p.Arg358=)	rs6067	0.04455
NM_000173.7(GP1BA):c.1282_1359del (p.415_427SEPAPSPTTPEPT[1])	rs869060239
NM_000173.7(GP1BA):c.1305_1320del (p.Thr436fs)	rs758041497
NM_000173.7(GP1BA):c.1311_1349del (p.415_427SEPAPSPTTPEPT[2])	rs770991996

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