List of variants studied for Neurofibromatosis, type 2 by OMIM

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
		ClinVar version:

Total variants: 14

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HGVS	dbSNP	gnomAD frequency
NM_000268.4(NF2):c.1021C>T (p.Arg341Ter)	rs74315499
NM_000268.4(NF2):c.1079T>C (p.Leu360Pro)	rs74315492
NM_000268.4(NF2):c.1219C>T (p.Gln407Ter)	rs74315501
NM_000268.4(NF2):c.1387G>T (p.Glu463Ter)	rs74315503
NM_000268.4(NF2):c.1396C>T (p.Arg466Ter)	rs74315504
NM_000268.4(NF2):c.1579G>T (p.Glu527Ter)	rs74315505
NM_000268.4(NF2):c.1604T>C (p.Leu535Pro)	rs74315493
NM_000268.4(NF2):c.1613A>C (p.Gln538Pro)	rs74315494
NM_000268.4(NF2):c.185T>C (p.Phe62Ser)	rs121434261
NM_000268.4(NF2):c.240+1G>T	rs587776562
NM_000268.4(NF2):c.285CTT[1] (p.Phe96del)	rs121434260
NM_000268.4(NF2):c.544G>T (p.Glu182Ter)	rs74315495
NM_000268.4(NF2):c.784C>T (p.Arg262Ter)	rs74315496
NM_000268.4(NF2):c.958C>T (p.Gln320Ter)	rs74315497

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