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rs1064795818

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Chromosome1
Position12002021
GeneMFN2
is asnp
is mentioned by
dbSNPrs1064795818
dbSNP (old)rs1064795818
ClinGenrs1064795818
ebirs1064795818
HLIrs1064795818
Exacrs1064795818
Gnomadrs1064795818
Varsomers1064795818
Maprs1064795818
PheGenIrs1064795818
Biobankrs1064795818
1000 genomesrs1064795818
hgdprs1064795818
ensemblrs1064795818
gopubmedrs1064795818
geneviewrs1064795818
scholarrs1064795818
googlers1064795818
pharmgkbrs1064795818
gwascentralrs1064795818
openSNPrs1064795818
23andMers1064795818
23andMe allrs1064795818
SNPshotrs1064795818
SNPdbers1064795818
MSV3drs1064795818
GWAS Ctlgrs1064795818
Max Magnitude0
ClinVar
Risk rs1064795818(G;G)
Alt rs1064795818(G;G)
Reference Rs1064795818(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MFN2
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.12062078C>G
CLNSRC
CLNACC RCV000486402.1,