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rs112039851

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs112039851(C;C)
Make rs112039851(C;G)
ReferenceGRCh38.p2 38.2/144
Chromosome1
Position1045444
GeneAGRN
is asnp
is mentioned by
dbSNPrs112039851
ebirs112039851
HLIrs112039851
Exacrs112039851
Varsomers112039851
Maprs112039851
PheGenIrs112039851
hapmaprs112039851
1000 genomesrs112039851
hgdprs112039851
ensemblrs112039851
gopubmedrs112039851
geneviewrs112039851
scholarrs112039851
googlers112039851
pharmgkbrs112039851
gwascentralrs112039851
openSNPrs112039851
23andMers112039851
23andMe allrs112039851
SNP Nexus

SNPshotrs112039851
SNPdbers112039851
MSV3drs112039851
GWAS Ctlgrs112039851
Max Magnitude0
ClinVar
Risk rs112039851(A,C;A,C)
Alt rs112039851(A,C;A,C)
Reference rs112039851(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene AGRN
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.980824G>C
CLNSRC
CLNACC RCV000171144.1,