List of variants in gene combination LOC130009809, RNASEH2B reported as uncertain significance for immune system disorder

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Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 8

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HGVS	dbSNP	gnomAD frequency
NM_001142279.2(RNASEH2B):c.-399C>G	rs553965425	0.00165
NM_024570.4(RNASEH2B):c.-228C>A	rs577725827	0.00051
NM_024570.4(RNASEH2B):c.-145G>A	rs1227696445	0.00003
NM_024570.4(RNASEH2B):c.-181G>A	rs886050288	0.00001
NM_001142279.2(RNASEH2B):c.-293A>G	rs1879223372
NM_001142279.2(RNASEH2B):c.-294C>T	rs1879223150
NM_001142279.2(RNASEH2B):c.-313C>G	rs886050287
NM_024570.4(RNASEH2B):c.-107G>A	rs886050289

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