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rs863224066

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs863224066(C;T)
Make rs863224066(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position12001482
GeneMFN2
is asnp
is mentioned by
dbSNPrs863224066
ebirs863224066
HLIrs863224066
Exacrs863224066
Varsomers863224066
Maprs863224066
PheGenIrs863224066
hapmaprs863224066
1000 genomesrs863224066
hgdprs863224066
ensemblrs863224066
gopubmedrs863224066
geneviewrs863224066
scholarrs863224066
googlers863224066
pharmgkbrs863224066
gwascentralrs863224066
openSNPrs863224066
23andMers863224066
23andMe allrs863224066
SNP Nexus

SNPshotrs863224066
SNPdbers863224066
MSV3drs863224066
GWAS Ctlgrs863224066
Max Magnitude0
ClinVar
Risk rs863224066(T;T)
Alt rs863224066(T;T)
Reference rs863224066(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MFN2
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.12061539C>T
CLNSRC
CLNACC RCV000195483.2,