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rs267607508

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs267607508(A;A)
Make rs267607508(A;C)
ReferenceGRCh38.p2 38.2/146
Chromosome17
Position44908128
GeneGFAP
is asnp
is mentioned by
dbSNPrs267607508
ebirs267607508
HLIrs267607508
Exacrs267607508
Varsomers267607508
Maprs267607508
PheGenIrs267607508
hapmaprs267607508
1000 genomesrs267607508
hgdprs267607508
ensemblrs267607508
gopubmedrs267607508
geneviewrs267607508
scholarrs267607508
googlers267607508
pharmgkbrs267607508
gwascentralrs267607508
openSNPrs267607508
23andMers267607508
23andMe allrs267607508
SNP Nexus

SNPshotrs267607508
SNPdbers267607508
MSV3drs267607508
GWAS Ctlgrs267607508
Max Magnitude0
ClinVar
Risk rs267607508(A;A)
Alt rs267607508(A;A)
Reference rs267607508(C;C)
Significance Pathogenic
Disease Alexander's disease not provided
Variation info
Gene GFAP
CLNDBN Alexander's disease not provided
Reversed 1
HGVS NC_000017.10:g.42985496G>A; NC_000017.10:g.42985496G>T
CLNSRC
CLNACC RCV000192183.1, RCV000056847.1, RCV000192184.1,