List of variants in gene combination LOC130009810, RNASEH2B reported as likely benign for immune system disorder

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 19

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HGVS	dbSNP	gnomAD frequency
NM_024570.4(RNASEH2B):c.64+8C>T	rs957777357	0.00018
NM_024570.4(RNASEH2B):c.55C>T (p.Leu19=)	rs1181798662	0.00003
NM_024570.4(RNASEH2B):c.39C>T (p.Ala13=)	rs571566229	0.00001
NM_024570.4(RNASEH2B):c.12C>G (p.Gly4=)
NM_024570.4(RNASEH2B):c.15G>T (p.Val5=)
NM_024570.4(RNASEH2B):c.18C>T (p.Asp6=)	rs2137866261
NM_024570.4(RNASEH2B):c.21C>T (p.Cys7=)
NM_024570.4(RNASEH2B):c.30G>A (p.Gly10=)	rs1244567393
NM_024570.4(RNASEH2B):c.54C>T (p.Phe18=)	rs2137866619
NM_024570.4(RNASEH2B):c.64+11G>A
NM_024570.4(RNASEH2B):c.64+11G>T
NM_024570.4(RNASEH2B):c.64+13G>T
NM_024570.4(RNASEH2B):c.64+14C>T
NM_024570.4(RNASEH2B):c.64+16C>G
NM_024570.4(RNASEH2B):c.64+16C>T	rs1321434798
NM_024570.4(RNASEH2B):c.64+17G>A	rs1451402273
NM_024570.4(RNASEH2B):c.64+7_64+8del
NM_024570.4(RNASEH2B):c.6C>G (p.Ala2=)
NM_024570.4(RNASEH2B):c.9T>G (p.Ala3=)

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