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rs62636501

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs62636501(A;T)
Make rs62636501(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome17
Position44911284
GeneGFAP
is asnp
is mentioned by
dbSNPrs62636501
ebirs62636501
HLIrs62636501
Exacrs62636501
Varsomers62636501
Maprs62636501
PheGenIrs62636501
hapmaprs62636501
1000 genomesrs62636501
hgdprs62636501
ensemblrs62636501
gopubmedrs62636501
geneviewrs62636501
scholarrs62636501
googlers62636501
pharmgkbrs62636501
gwascentralrs62636501
openSNPrs62636501
23andMers62636501
23andMe allrs62636501
SNP Nexus

SNPshotrs62636501
SNPdbers62636501
MSV3drs62636501
GWAS Ctlgrs62636501
Max Magnitude0
ClinVar
Risk rs62636501(T;T)
Alt rs62636501(T;T)
Reference rs62636501(A;A)
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.42988652T>A
CLNSRC
CLNACC RCV000056824.1, RCV000192162.1,