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rs1057517987

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057517987(C;T)
Make rs1057517987(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome1
Position12004083
GeneMFN2
is asnp
is mentioned by
dbSNPrs1057517987
dbSNP (old)rs1057517987
ClinGenrs1057517987
ebirs1057517987
HLIrs1057517987
Exacrs1057517987
Gnomadrs1057517987
Varsomers1057517987
Maprs1057517987
PheGenIrs1057517987
Biobankrs1057517987
1000 genomesrs1057517987
hgdprs1057517987
ensemblrs1057517987
gopubmedrs1057517987
geneviewrs1057517987
scholarrs1057517987
googlers1057517987
pharmgkbrs1057517987
gwascentralrs1057517987
openSNPrs1057517987
23andMers1057517987
23andMe allrs1057517987
SNPshotrs1057517987
SNPdbers1057517987
MSV3drs1057517987
GWAS Ctlgrs1057517987
Max Magnitude0
ClinVar
Risk rs1057517987(T;T)
Alt rs1057517987(T;T)
Reference Rs1057517987(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MFN2
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.12064140C>T
CLNSRC
CLNACC RCV000413487.1,