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rs76264143

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs76264143(C;C)
Make rs76264143(C;G)
ReferenceGRCh38.p2 38.2/144
Chromosome1
Position1047464
GeneAGRN
is asnp
is mentioned by
dbSNPrs76264143
ebirs76264143
HLIrs76264143
Exacrs76264143
Varsomers76264143
Maprs76264143
PheGenIrs76264143
hapmaprs76264143
1000 genomesrs76264143
hgdprs76264143
ensemblrs76264143
gopubmedrs76264143
geneviewrs76264143
scholarrs76264143
googlers76264143
pharmgkbrs76264143
gwascentralrs76264143
openSNPrs76264143
23andMers76264143
23andMe allrs76264143
SNP Nexus

SNPshotrs76264143
SNPdbers76264143
MSV3drs76264143
GWAS Ctlgrs76264143
Max Magnitude0
ClinVar
Risk rs76264143(C;C)
Alt rs76264143(C;C)
Reference rs76264143(G;G)
Significance Probable-Pathogenic
Disease not specified not provided
Variation info
Gene AGRN
CLNDBN not specified not provided
Reversed 0
HGVS NC_000001.10:g.982844G>C
CLNSRC
CLNACC RCV000116263.2, RCV000171145.1,