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rs879253777

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs879253777(G;T)
Make rs879253777(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome1
Position11999009
GeneMFN2
is asnp
is mentioned by
dbSNPrs879253777
ebirs879253777
HLIrs879253777
Exacrs879253777
Varsomers879253777
Maprs879253777
PheGenIrs879253777
hapmaprs879253777
1000 genomesrs879253777
hgdprs879253777
ensemblrs879253777
gopubmedrs879253777
geneviewrs879253777
scholarrs879253777
googlers879253777
pharmgkbrs879253777
gwascentralrs879253777
openSNPrs879253777
23andMers879253777
23andMe allrs879253777
SNP Nexus

SNPshotrs879253777
SNPdbers879253777
MSV3drs879253777
GWAS Ctlgrs879253777
Max Magnitude0
ClinVar
Risk rs879253777(A,T;A,T)
Alt rs879253777(A,T;A,T)
Reference rs879253777(G;G)
Significance Pathogenic
Disease Charcot-Marie-Tooth disease
Variation info
Gene MFN2
CLNDBN Charcot-Marie-Tooth disease, type 2A2
Reversed 0
HGVS NC_000001.10:g.12059066G>A; NC_000001.10:g.12059066G>T
CLNSRC
CLNACC RCV000235053.1, RCV000235088.1,