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rs863224068

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs863224068(G;T)
Make rs863224068(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position11992690
GeneMFN2
is asnp
is mentioned by
dbSNPrs863224068
ebirs863224068
HLIrs863224068
Exacrs863224068
Varsomers863224068
Maprs863224068
PheGenIrs863224068
hapmaprs863224068
1000 genomesrs863224068
hgdprs863224068
ensemblrs863224068
gopubmedrs863224068
geneviewrs863224068
scholarrs863224068
googlers863224068
pharmgkbrs863224068
gwascentralrs863224068
openSNPrs863224068
23andMers863224068
23andMe allrs863224068
SNP Nexus

SNPshotrs863224068
SNPdbers863224068
MSV3drs863224068
GWAS Ctlgrs863224068
Max Magnitude0
ClinVar
Risk rs863224068(T;T)
Alt rs863224068(T;T)
Reference rs863224068(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene MFN2
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.12052747G>T
CLNSRC
CLNACC RCV000196210.1,