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rs863224064

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs863224064(A;A)
Make rs863224064(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position11997363
GeneMFN2
is asnp
is mentioned by
dbSNPrs863224064
ebirs863224064
HLIrs863224064
Exacrs863224064
Varsomers863224064
Maprs863224064
PheGenIrs863224064
hapmaprs863224064
1000 genomesrs863224064
hgdprs863224064
ensemblrs863224064
gopubmedrs863224064
geneviewrs863224064
scholarrs863224064
googlers863224064
pharmgkbrs863224064
gwascentralrs863224064
openSNPrs863224064
23andMers863224064
23andMe allrs863224064
SNP Nexus

SNPshotrs863224064
SNPdbers863224064
MSV3drs863224064
GWAS Ctlgrs863224064
Max Magnitude0
ClinVar
Risk rs863224064(A;A)
Alt rs863224064(A;A)
Reference rs863224064(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MFN2
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.12057420G>A
CLNSRC
CLNACC RCV000199084.2,