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rs12069578

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs12069578(A;A)
Make rs12069578(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome1
Position12004010
GeneMFN2
is asnp
is mentioned by
dbSNPrs12069578
ebirs12069578
HLIrs12069578
Exacrs12069578
Varsomers12069578
Maprs12069578
PheGenIrs12069578
hapmaprs12069578
1000 genomesrs12069578
hgdprs12069578
ensemblrs12069578
gopubmedrs12069578
geneviewrs12069578
scholarrs12069578
googlers12069578
pharmgkbrs12069578
gwascentralrs12069578
openSNPrs12069578
23andMers12069578
23andMe allrs12069578
SNP Nexus

SNPshotrs12069578
SNPdbers12069578
MSV3drs12069578
GWAS Ctlgrs12069578
Max Magnitude0
? (A;A) (A;G) (G;G) 28
ClinVar
Risk rs12069578(A,C;A,C)
Alt rs12069578(A,C;A,C)
Reference rs12069578(G;G)
Significance Pathogenic
Disease not specified not provided
Variation info
Gene MFN2
CLNDBN not specified not provided
Reversed 0
HGVS NC_000001.10:g.12064067G>A
CLNSRC
CLNACC RCV000174373.3, RCV000212509.1,