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rs61726470

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs61726470(C;G)
Make rs61726470(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome17
Position44913291
GeneGFAP
is asnp
is mentioned by
dbSNPrs61726470
ebirs61726470
HLIrs61726470
Exacrs61726470
Varsomers61726470
Maprs61726470
PheGenIrs61726470
hapmaprs61726470
1000 genomesrs61726470
hgdprs61726470
ensemblrs61726470
gopubmedrs61726470
geneviewrs61726470
scholarrs61726470
googlers61726470
pharmgkbrs61726470
gwascentralrs61726470
openSNPrs61726470
23andMers61726470
23andMe allrs61726470
SNP Nexus

SNPshotrs61726470
SNPdbers61726470
MSV3drs61726470
GWAS Ctlgrs61726470
Max Magnitude0
ClinVar
Risk rs61726470(G;G)
Alt rs61726470(G;G)
Reference rs61726470(C;C)
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.42990659G>C
CLNSRC
CLNACC RCV000056905.1, RCV000192141.1,