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rs121909719

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121909719(G;T)
Make rs121909719(T;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position44911751
GeneGFAP
is asnp
is mentioned by
dbSNPrs121909719
ebirs121909719
HLIrs121909719
Exacrs121909719
Varsomers121909719
Maprs121909719
PheGenIrs121909719
hapmaprs121909719
1000 genomesrs121909719
hgdprs121909719
ensemblrs121909719
gopubmedrs121909719
geneviewrs121909719
scholarrs121909719
googlers121909719
pharmgkbrs121909719
gwascentralrs121909719
openSNPrs121909719
23andMers121909719
23andMe allrs121909719
SNP Nexus

SNPshotrs121909719
SNPdbers121909719
MSV3drs121909719
GWAS Ctlgrs121909719
Merged fromRs28933071
Max Magnitude0
OMIM137780
Desc
Variant0011
Relatedalso
ClinVar
Risk rs121909719(T;T)
Alt rs121909719(T;T)
Reference rs121909719(G;G)
Significance Pathogenic
Disease Alexander's disease not provided
Variation info
Gene GFAP
CLNDBN Alexander's disease not provided
Reversed 1
HGVS NC_000017.10:g.42989119C>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000017560.29, RCV000056910.1,