List of variants reported as likely benign for multiple sclerosis

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Total variants: 7

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HGVS	dbSNP	gnomAD frequency
NM_031157.4(HNRNPA1):c.1078T>G (p.Ser360Ala)	rs483353040
NM_031157.4(HNRNPA1):c.1093A>G (p.Ser365Gly)	rs483353026
NM_031157.4(HNRNPA1):c.1096T>C (p.Tyr366His)	rs483353027
NM_031157.4(HNRNPA1):c.1097A>G (p.Tyr366Cys)	rs483353041
NM_031157.4(HNRNPA1):c.1106G>A (p.Gly369Asp)	rs483353042
NM_031157.4(HNRNPA1):c.1111A>G (p.Arg371Gly)	rs3206707
NM_031157.4(HNRNPA1):c.1114T>C (p.Phe372Leu)	rs483353043

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