List of variants in gene PLXNA2 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: 6

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HGVS	dbSNP	gnomAD frequency
NM_025179.4(PLXNA2):c.365C>A (p.Ser122Tyr)	rs142871447	0.00599
NM_025179.4(PLXNA2):c.1867G>A (p.Val623Ile)	rs150558490	0.00503
NM_025179.4(PLXNA2):c.5334C>T (p.Phe1778=)	rs113155197	0.00324
NM_025179.4(PLXNA2):c.1488C>T (p.Tyr496=)	rs149871348	0.00236
NM_025179.4(PLXNA2):c.3451A>G (p.Thr1151Ala)	rs138766213	0.00081
NM_025179.4(PLXNA2):c.2595G>A (p.Thr865=)

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