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rs61060395

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs61060395(G;G)
Make rs61060395(G;T)
ReferenceGRCh38.p2 38.2/146
Chromosome17
Position44915269
GeneGFAP
is asnp
is mentioned by
dbSNPrs61060395
ebirs61060395
HLIrs61060395
Exacrs61060395
Varsomers61060395
Maprs61060395
PheGenIrs61060395
hapmaprs61060395
1000 genomesrs61060395
hgdprs61060395
ensemblrs61060395
gopubmedrs61060395
geneviewrs61060395
scholarrs61060395
googlers61060395
pharmgkbrs61060395
gwascentralrs61060395
openSNPrs61060395
23andMers61060395
23andMe allrs61060395
SNP Nexus

SNPshotrs61060395
SNPdbers61060395
MSV3drs61060395
GWAS Ctlgrs61060395
Max Magnitude0
ClinVar
Risk rs61060395(A,G;A,G)
Alt rs61060395(A,G;A,G)
Reference rs61060395(T;T)
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.42992637A>C; NC_000017.10:g.42992637A>G; NC_000017.10:g.42992637A>T
CLNSRC
CLNACC RCV000056860.1, RCV000192104.1, RCV000192103.1, RCV000056859.1, RCV000192105.1,