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rs397515479

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397515479(C;T)
Make rs397515479(T;T)
ReferenceGRCh38 38.1/141
Chromosome19
Position12806748
GeneRNASEH2A
is asnp
is mentioned by
dbSNPrs397515479
ebirs397515479
HLIrs397515479
Exacrs397515479
Varsomers397515479
Maprs397515479
PheGenIrs397515479
hapmaprs397515479
1000 genomesrs397515479
hgdprs397515479
ensemblrs397515479
gopubmedrs397515479
geneviewrs397515479
scholarrs397515479
googlers397515479
pharmgkbrs397515479
gwascentralrs397515479
openSNPrs397515479
23andMers397515479
23andMe allrs397515479
SNP Nexus

SNPshotrs397515479
SNPdbers397515479
MSV3drs397515479
GWAS Ctlgrs397515479
Max Magnitude0
ClinVar
Risk rs397515479(T;T)
Alt rs397515479(T;T)
Reference rs397515479(C;C)
Significance Pathogenic
Disease Aicardi Goutieres syndrome 4
Variation info
Gene RNASEH2A
CLNDBN Aicardi Goutieres syndrome 4
Reversed 0
HGVS NC_000019.9:g.12917562C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000056302.5,