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rs4792938

From SNPedia

Orientationplus
Stabilizedplus
Make rs4792938(C;C)
Make rs4792938(C;G)
Make rs4792938(G;G)
ReferenceGRCh38 38.1/141
Chromosome17
Position44347231
GeneGRN
is asnp
is mentioned by
dbSNPrs4792938
ebirs4792938
HLIrs4792938
Exacrs4792938
Varsomers4792938
Maprs4792938
PheGenIrs4792938
hapmaprs4792938
1000 genomesrs4792938
hgdprs4792938
ensemblrs4792938
gopubmedrs4792938
geneviewrs4792938
scholarrs4792938
googlers4792938
pharmgkbrs4792938
gwascentralrs4792938
openSNPrs4792938
23andMers4792938
23andMe allrs4792938
SNP Nexus

SNPshotrs4792938
SNPdbers4792938
MSV3drs4792938
GWAS Ctlgrs4792938
GMAF0.4086
Max Magnitude
? (C;C) (C;G) (G;G) 28

[PMID 20061636] GRN variability contributes to sporadic frontotemporal lobar degeneration [PMID 20463744] Progranulin gene variability increases the risk for primary progressive multiple sclerosis in males.

[PMID 24581833] Further evidence for plasma progranulin as a biomarker in bipolar disorder