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rs1057519024

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1057519024(A;A)
Make rs1057519024(A;T)
ReferenceGRCh38.p7 38.3/150
Chromosome3
Position155116561
GeneMME
is asnp
is mentioned by
dbSNPrs1057519024
dbSNP (old)rs1057519024
ClinGenrs1057519024
ebirs1057519024
HLIrs1057519024
Exacrs1057519024
Gnomadrs1057519024
Varsomers1057519024
Maprs1057519024
PheGenIrs1057519024
Biobankrs1057519024
1000 genomesrs1057519024
hgdprs1057519024
ensemblrs1057519024
gopubmedrs1057519024
geneviewrs1057519024
scholarrs1057519024
googlers1057519024
pharmgkbrs1057519024
gwascentralrs1057519024
openSNPrs1057519024
23andMers1057519024
23andMe allrs1057519024
SNPshotrs1057519024
SNPdbers1057519024
MSV3drs1057519024
GWAS Ctlgrs1057519024
Max Magnitude0
ClinVar
Risk rs1057519024(A;A)
Alt rs1057519024(A;A)
Reference Rs1057519024(T;T)
Significance Pathogenic
Disease Charcot-Marie-Tooth disease
Variation info
Gene MME
CLNDBN Charcot-Marie-Tooth disease, axonal, type 2T
Reversed 0
HGVS NC_000003.11:g.154834350T>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000234893.1,