List of variants reported as likely pathogenic for multiple sclerosis

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Total variants: 14

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HGVS	dbSNP	gnomAD frequency
NM_031157.4(HNRNPA1):c.949A>G (p.Asn317Asp)	rs483353023	0.00001
NM_031157.4(HNRNPA1):c.1006A>G (p.Arg336Gly)	rs483353032
NM_031157.4(HNRNPA1):c.1009A>G (p.Ser337Gly)	rs483353033
NM_031157.4(HNRNPA1):c.1040A>G (p.Tyr347Cys)	rs483353034
NM_031157.4(HNRNPA1):c.1042T>C (p.Phe348Leu)	rs483353035
NM_031157.4(HNRNPA1):c.1052C>T (p.Pro351Leu)	rs483353036
NM_031157.4(HNRNPA1):c.1054C>T (p.Arg352Ter)	rs483353037
NM_031157.4(HNRNPA1):c.1057A>G (p.Asn353Asp)	rs483353039
NM_031157.4(HNRNPA1):c.1058A>G (p.Asn353Ser)	rs483353038
NM_031157.4(HNRNPA1):c.943T>C (p.Phe315Leu)	rs483353022
NM_031157.4(HNRNPA1):c.979C>T (p.Pro327Ser)	rs483353029
NM_031157.4(HNRNPA1):c.982A>C (p.Met328Leu)	rs483353024
NM_031157.4(HNRNPA1):c.987G>T (p.Lys329Asn)	rs483353030
NM_031157.4(HNRNPA1):c.995A>G (p.Asn332Ser)	rs3207617

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