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rs863224065

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs863224065(A;G)
Make rs863224065(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position11999004
GeneMFN2
is asnp
is mentioned by
dbSNPrs863224065
ebirs863224065
HLIrs863224065
Exacrs863224065
Varsomers863224065
Maprs863224065
PheGenIrs863224065
hapmaprs863224065
1000 genomesrs863224065
hgdprs863224065
ensemblrs863224065
gopubmedrs863224065
geneviewrs863224065
scholarrs863224065
googlers863224065
pharmgkbrs863224065
gwascentralrs863224065
openSNPrs863224065
23andMers863224065
23andMe allrs863224065
SNP Nexus

SNPshotrs863224065
SNPdbers863224065
MSV3drs863224065
GWAS Ctlgrs863224065
Max Magnitude0
ClinVar
Risk rs863224065(G;G)
Alt rs863224065(G;G)
Reference rs863224065(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MFN2
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.12059061A>G
CLNSRC
CLNACC RCV000195514.1,