ClinVar Miner

List of variants in gene HNRNPA1 reported as uncertain significance for multiple sclerosis

Included ClinVar conditions (4):

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: 2

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HGVS	dbSNP	gnomAD frequency
NM_031157.4(HNRNPA1):c.911G>A (p.Ser304Asn)	rs483353020	0.00003
NM_031157.4(HNRNPA1):c.931A>G (p.Ser311Gly)	rs483353021

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