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rs1060501925

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1060501925(G;T)
Make rs1060501925(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome1
Position12011511
GeneMFN2
is asnp
is mentioned by
dbSNPrs1060501925
dbSNP (old)rs1060501925
ClinGenrs1060501925
ebirs1060501925
HLIrs1060501925
Exacrs1060501925
Gnomadrs1060501925
Varsomers1060501925
LitVarrs1060501925
Maprs1060501925
PheGenIrs1060501925
Biobankrs1060501925
1000 genomesrs1060501925
hgdprs1060501925
ensemblrs1060501925
gopubmedrs1060501925
geneviewrs1060501925
scholarrs1060501925
googlers1060501925
pharmgkbrs1060501925
gwascentralrs1060501925
openSNPrs1060501925
23andMers1060501925
23andMe allrs1060501925
SNPshotrs1060501925
SNPdbers1060501925
MSV3drs1060501925
GWAS Ctlgrs1060501925
Max Magnitude0
ClinVar
Risk rs1060501925(T;T)
Alt rs1060501925(T;T)
Reference Rs1060501925(G;G)
Significance Probable-Pathogenic
Disease Charcot-Marie-Tooth disease
Variation info
Gene MFN2
CLNDBN Charcot-Marie-Tooth disease, type 2
Reversed 0
HGVS NC_000001.10:g.12071568G>T
CLNSRC
CLNACC RCV000458069.1,