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rs768943773

From SNPedia

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Geno Mag Summary
(G;G) 0 common in clinvar
Make rs768943773(G;T)
Make rs768943773(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome1
Position154598557
GeneADAR
is asnp
is mentioned by
dbSNPrs768943773
ebirs768943773
HLIrs768943773
Exacrs768943773
Varsomers768943773
Maprs768943773
PheGenIrs768943773
hapmaprs768943773
1000 genomesrs768943773
hgdprs768943773
ensemblrs768943773
gopubmedrs768943773
geneviewrs768943773
scholarrs768943773
googlers768943773
pharmgkbrs768943773
gwascentralrs768943773
openSNPrs768943773
23andMers768943773
23andMe allrs768943773
SNP Nexus

SNPshotrs768943773
SNPdbers768943773
MSV3drs768943773
GWAS Ctlgrs768943773
Max Magnitude0
ClinVar
Risk rs768943773(T;T)
Alt rs768943773(T;T)
Reference rs768943773(G;G)
Significance Pathogenic
Disease Aicardi-goutieres syndrome 6
Variation info
Gene ADAR
CLNDBN Aicardi-goutieres syndrome 6
Reversed 0
HGVS NC_000001.10:g.154571033G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000114429.2,