ClinVar Miner

List of variants in gene RNASEH2B reported as likely benign for Aicardi-Goutieres syndrome

Included ClinVar conditions (15):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 11
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HGVS dbSNP
NM_001142279.2(RNASEH2B):c.-112C>T rs184573722
NM_001142279.2(RNASEH2B):c.-117C>G rs553446261
NM_001142279.2(RNASEH2B):c.156G>A (p.Leu52=) rs35416748
NM_001142279.2(RNASEH2B):c.455A>G (p.Asn152Ser) rs146451037
NM_001142279.2(RNASEH2B):c.741+4414A>G rs200721645
NM_001142279.2(RNASEH2B):c.741+6955dup rs75254367
NM_024570.4(RNASEH2B):c.203A>G (p.Glu68Gly) rs148811739
NM_024570.4(RNASEH2B):c.240A>G (p.Gln80=) rs781187392
NM_024570.4(RNASEH2B):c.64+8C>T rs957777357
NM_024570.4(RNASEH2B):c.762G>A (p.Glu254=) rs146378238
NM_024570.4(RNASEH2B):c.895A>G (p.Thr299Ala) rs370507842

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