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rs59628143

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs59628143(A;G)
Make rs59628143(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome17
Position44911242
GeneGFAP
is asnp
is mentioned by
dbSNPrs59628143
ebirs59628143
HLIrs59628143
Exacrs59628143
Varsomers59628143
Maprs59628143
PheGenIrs59628143
hapmaprs59628143
1000 genomesrs59628143
hgdprs59628143
ensemblrs59628143
gopubmedrs59628143
geneviewrs59628143
scholarrs59628143
googlers59628143
pharmgkbrs59628143
gwascentralrs59628143
openSNPrs59628143
23andMers59628143
23andMe allrs59628143
SNP Nexus

SNPshotrs59628143
SNPdbers59628143
MSV3drs59628143
GWAS Ctlgrs59628143
Max Magnitude0
ClinVar
Risk rs59628143(G;G)
Alt rs59628143(G;G)
Reference rs59628143(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.42988610T>C
CLNSRC
CLNACC RCV000056835.1, RCV000192176.1,