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rs797044580

From SNPedia

Orientationminus
Make rs797044580(CT;CT)
Make rs797044580(CT;TG)
ReferenceGRCh38.p2 38.2/146
Chromosome17
Position44911786
GeneGFAP
is asnp
is mentioned by
dbSNPrs797044580
ebirs797044580
HLIrs797044580
Exacrs797044580
Varsomers797044580
Maprs797044580
PheGenIrs797044580
hapmaprs797044580
1000 genomesrs797044580
hgdprs797044580
ensemblrs797044580
gopubmedrs797044580
geneviewrs797044580
scholarrs797044580
googlers797044580
pharmgkbrs797044580
gwascentralrs797044580
openSNPrs797044580
23andMers797044580
23andMe allrs797044580
SNP Nexus

SNPshotrs797044580
SNPdbers797044580
MSV3drs797044580
GWAS Ctlgrs797044580
Max Magnitude
ClinVar
Risk rs797044580(CT;CT)
Alt rs797044580(CT;CT)
Reference rs797044580(TG;TG)
Significance Pathogenic
Disease Alexander's disease
Variation info
Gene GFAP
CLNDBN Alexander's disease
Reversed 1
HGVS NC_000017.10:g.42989154_42989155delCAinsAG
CLNSRC
CLNACC RCV000192146.1,