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rs1064793170

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Chromosome1
Position12002025
GeneMFN2
is asnp
is mentioned by
dbSNPrs1064793170
dbSNP (old)rs1064793170
ClinGenrs1064793170
ebirs1064793170
HLIrs1064793170
Exacrs1064793170
Gnomadrs1064793170
Varsomers1064793170
Maprs1064793170
PheGenIrs1064793170
Biobankrs1064793170
1000 genomesrs1064793170
hgdprs1064793170
ensemblrs1064793170
gopubmedrs1064793170
geneviewrs1064793170
scholarrs1064793170
googlers1064793170
pharmgkbrs1064793170
gwascentralrs1064793170
openSNPrs1064793170
23andMers1064793170
23andMe allrs1064793170
SNPshotrs1064793170
SNPdbers1064793170
MSV3drs1064793170
GWAS Ctlgrs1064793170
Max Magnitude0
ClinVar
Risk rs1064793170(G;G)
Alt rs1064793170(G;G)
Reference Rs1064793170(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MFN2
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.12062082A>G
CLNSRC
CLNACC RCV000485629.1,