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rs59985777

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs59985777(C;C)
Make rs59985777(C;T)
ReferenceGRCh38.p2 38.2/146
Chromosome17
Position44911371
GeneGFAP
is asnp
is mentioned by
dbSNPrs59985777
ClinGenrs59985777
ebirs59985777
HLIrs59985777
Exacrs59985777
Varsomers59985777
Maprs59985777
PheGenIrs59985777
hapmaprs59985777
1000 genomesrs59985777
hgdprs59985777
ensemblrs59985777
gopubmedrs59985777
geneviewrs59985777
scholarrs59985777
googlers59985777
pharmgkbrs59985777
gwascentralrs59985777
openSNPrs59985777
23andMers59985777
23andMe allrs59985777
SNP Nexus

SNPshotrs59985777
SNPdbers59985777
MSV3drs59985777
GWAS Ctlgrs59985777
Max Magnitude0
ClinVar
Risk rs59985777(C;C)
Alt rs59985777(C;C)
Reference Rs59985777(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.42988739A>G
CLNSRC
CLNACC RCV000056918.1, RCV000192153.1,