ClinVar Miner

List of variants in gene LOC130009809, RNASEH2B studied for autoinflammatory syndrome of childhood

Included ClinVar conditions (48):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 11
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HGVS dbSNP gnomAD frequency
NM_024570.4(RNASEH2B):c.-210G>C rs112702177 0.02962
NM_024570.4(RNASEH2B):c.-112C>T rs184573722 0.00678
NM_001142279.2(RNASEH2B):c.-399C>G rs553965425 0.00165
NM_024570.4(RNASEH2B):c.-117C>G rs553446261 0.00094
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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