List of variants in gene HNRNPA1 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_031157.4(HNRNPA1):c.546A>G (p.Ser182=)	rs200707918	0.00076
NM_031157.4(HNRNPA1):c.1064-31_1064-24del
NM_031157.4(HNRNPA1):c.447C>T (p.Ala149=)	rs199853948
NM_031157.4(HNRNPA1):c.507T>G (p.Thr169=)	rs1349265535
NM_031157.4(HNRNPA1):c.676+35C>G	rs187988364
NM_031157.4(HNRNPA1):c.786A>T (p.Gly262=)	rs2540584009

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