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rs398122892

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs398122892(A;A)
Make rs398122892(A;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position154589456
GeneADAR
is asnp
is mentioned by
dbSNPrs398122892
ebirs398122892
HLIrs398122892
Exacrs398122892
Varsomers398122892
Maprs398122892
PheGenIrs398122892
hapmaprs398122892
1000 genomesrs398122892
hgdprs398122892
ensemblrs398122892
gopubmedrs398122892
geneviewrs398122892
scholarrs398122892
googlers398122892
pharmgkbrs398122892
gwascentralrs398122892
openSNPrs398122892
23andMers398122892
23andMe allrs398122892
SNP Nexus

SNPshotrs398122892
SNPdbers398122892
MSV3drs398122892
GWAS Ctlgrs398122892
Max Magnitude0
ClinVar
Risk rs398122892(A;A)
Alt rs398122892(A;A)
Reference rs398122892(G;G)
Significance Other
Disease Aicardi-goutieres syndrome 6
Variation info
Gene ADAR
CLNDBN Aicardi-goutieres syndrome 6
Reversed 1
HGVS NC_000001.10:g.154561932C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000032650.26,