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rs763868966

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs763868966(A;A)
Make rs763868966(A;C)
ReferenceGRCh38.p2 38.2/146
Chromosome17
Position44911429
GeneGFAP
is asnp
is mentioned by
dbSNPrs763868966
ebirs763868966
HLIrs763868966
Exacrs763868966
Varsomers763868966
Maprs763868966
PheGenIrs763868966
hapmaprs763868966
1000 genomesrs763868966
hgdprs763868966
ensemblrs763868966
gopubmedrs763868966
geneviewrs763868966
scholarrs763868966
googlers763868966
pharmgkbrs763868966
gwascentralrs763868966
openSNPrs763868966
23andMers763868966
23andMe allrs763868966
SNP Nexus

SNPshotrs763868966
SNPdbers763868966
MSV3drs763868966
GWAS Ctlgrs763868966
Max Magnitude0
ClinVar
Risk rs763868966(A,T;A,T)
Alt rs763868966(A,T;A,T)
Reference rs763868966(C;C)
Significance Pathogenic
Disease Alexander's disease
Variation info
Gene GFAP
CLNDBN Alexander's disease
Reversed 0
HGVS NC_000017.10:g.42988797C>A
CLNSRC
CLNACC RCV000192151.1,