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rs1064794316

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Chromosome1
Position12001414
GeneMFN2
is asnp
is mentioned by
dbSNPrs1064794316
dbSNP (old)rs1064794316
ClinGenrs1064794316
ebirs1064794316
HLIrs1064794316
Exacrs1064794316
Gnomadrs1064794316
Varsomers1064794316
Maprs1064794316
PheGenIrs1064794316
Biobankrs1064794316
1000 genomesrs1064794316
hgdprs1064794316
ensemblrs1064794316
gopubmedrs1064794316
geneviewrs1064794316
scholarrs1064794316
googlers1064794316
pharmgkbrs1064794316
gwascentralrs1064794316
openSNPrs1064794316
23andMers1064794316
23andMe allrs1064794316
SNPshotrs1064794316
SNPdbers1064794316
MSV3drs1064794316
GWAS Ctlgrs1064794316
Max Magnitude0
ClinVar
Risk rs1064794316(G;G)
Alt rs1064794316(G;G)
Reference Rs1064794316(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MFN2
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.12061471A>G
CLNSRC
CLNACC RCV000482327.1,