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rs398122822

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs398122822(A;A)
Make rs398122822(A;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position154588125
GeneADAR
is asnp
is mentioned by
dbSNPrs398122822
ebirs398122822
HLIrs398122822
Exacrs398122822
Varsomers398122822
Maprs398122822
PheGenIrs398122822
hapmaprs398122822
1000 genomesrs398122822
hgdprs398122822
ensemblrs398122822
gopubmedrs398122822
geneviewrs398122822
scholarrs398122822
googlers398122822
pharmgkbrs398122822
gwascentralrs398122822
openSNPrs398122822
23andMers398122822
23andMe allrs398122822
SNP Nexus

SNPshotrs398122822
SNPdbers398122822
MSV3drs398122822
GWAS Ctlgrs398122822
Max Magnitude0
ClinVar
Risk rs398122822(A;A)
Alt rs398122822(A;A)
Reference rs398122822(G;G)
Significance Other
Disease Symmetrical dyschromatosis of extremities Aicardi-goutieres syndrome 6
Variation info
Gene ADAR
CLNDBN Symmetrical dyschromatosis of extremities Aicardi-goutieres syndrome 6
Reversed 1
HGVS NC_000001.10:g.154560601C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000032653.27, RCV000032654.29,