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rs369762154

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs369762154(C;T)
Make rs369762154(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position12007167
GeneMFN2
is asnp
is mentioned by
dbSNPrs369762154
ebirs369762154
HLIrs369762154
Exacrs369762154
Varsomers369762154
Maprs369762154
PheGenIrs369762154
hapmaprs369762154
1000 genomesrs369762154
hgdprs369762154
ensemblrs369762154
gopubmedrs369762154
geneviewrs369762154
scholarrs369762154
googlers369762154
pharmgkbrs369762154
gwascentralrs369762154
openSNPrs369762154
23andMers369762154
23andMe allrs369762154
SNP Nexus

SNPshotrs369762154
SNPdbers369762154
MSV3drs369762154
GWAS Ctlgrs369762154
Max Magnitude0
ClinVar
Risk rs369762154(G,T;G,T)
Alt rs369762154(G,T;G,T)
Reference rs369762154(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MFN2
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.12067224C>T
CLNSRC
CLNACC RCV000197786.2,