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rs62635764

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs62635764(G;T)
Make rs62635764(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome17
Position44908143
GeneGFAP
is asnp
is mentioned by
dbSNPrs62635764
ebirs62635764
HLIrs62635764
Exacrs62635764
Varsomers62635764
Maprs62635764
PheGenIrs62635764
hapmaprs62635764
1000 genomesrs62635764
hgdprs62635764
ensemblrs62635764
gopubmedrs62635764
geneviewrs62635764
scholarrs62635764
googlers62635764
pharmgkbrs62635764
gwascentralrs62635764
openSNPrs62635764
23andMers62635764
23andMe allrs62635764
SNP Nexus

SNPshotrs62635764
SNPdbers62635764
MSV3drs62635764
GWAS Ctlgrs62635764
Max Magnitude0
ClinVar
Risk rs62635764(T;T)
Alt rs62635764(T;T)
Reference rs62635764(G;G)
Significance Pathogenic
Disease not provided Alexander's disease
Variation info
Gene GFAP
CLNDBN not provided Alexander's disease
Reversed 1
HGVS NC_000017.10:g.42985511C>A
CLNSRC
CLNACC RCV000056846.1, RCV000192182.1,