List of variants in gene NHP2 reported by Genetic Services Laboratory, University of Chicago

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 12

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HGVS	dbSNP	gnomAD frequency
NM_017838.4(NHP2):c.302G>A (p.Arg101Gln)	rs145890370	0.00615
NM_017838.4(NHP2):c.270A>G (p.Val90=)	rs148179279	0.00121
NM_017838.4(NHP2):c.190G>A (p.Val64Met)	rs79031130	0.00038
NM_017838.4(NHP2):c.-10G>T	rs371173524	0.00013
NM_017838.4(NHP2):c.109C>T (p.Pro37Ser)	rs201390429	0.00003
NM_017838.4(NHP2):c.289_290del (p.Met97fs)	rs762821341	0.00002
NM_017838.4(NHP2):c.-11C>T	rs764513273	0.00001
NM_017838.4(NHP2):c.-2C>A	rs1200196278	0.00001
NM_017838.4(NHP2):c.153C>G (p.Ile51Met)	rs771889761	0.00001
NM_017838.4(NHP2):c.160+9G>A	rs756638436	0.00001
NM_017838.4(NHP2):c.160+10A>T	rs376220034
NM_017838.4(NHP2):c.160+11C>T	rs201274409

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