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rs398122898

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(AGCGA;AGCGA) 0 common in clinvar
Make rs398122898(-;-)
Make rs398122898(-;AGCGA)
ReferenceGRCh38 38.1/141
Chromosome1
Position154601562
GeneADAR
is asnp
is mentioned by
dbSNPrs398122898
ebirs398122898
HLIrs398122898
Exacrs398122898
Varsomers398122898
Maprs398122898
PheGenIrs398122898
hapmaprs398122898
1000 genomesrs398122898
hgdprs398122898
ensemblrs398122898
gopubmedrs398122898
geneviewrs398122898
scholarrs398122898
googlers398122898
pharmgkbrs398122898
gwascentralrs398122898
openSNPrs398122898
23andMers398122898
23andMe allrs398122898
SNP Nexus

SNPshotrs398122898
SNPdbers398122898
MSV3drs398122898
GWAS Ctlgrs398122898
Max Magnitude0
ClinVar
Risk rs398122898(;)
Alt rs398122898(;)
Reference rs398122898(AGCGA;AGCGA)
Significance Pathogenic
Disease Aicardi-goutieres syndrome 6
Variation info
Gene ADAR
CLNDBN Aicardi-goutieres syndrome 6
Reversed 1
HGVS NC_000001.10:g.154574038_154574042delTCGCT
CLNSRC OMIM Allelic Variant
CLNACC RCV000032658.26,