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rs757563721

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs757563721(G;T)
Make rs757563721(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome11
Position95849835
GeneMTMR2
is asnp
is mentioned by
dbSNPrs757563721
ebirs757563721
HLIrs757563721
Exacrs757563721
Varsomers757563721
Maprs757563721
PheGenIrs757563721
hapmaprs757563721
1000 genomesrs757563721
hgdprs757563721
ensemblrs757563721
gopubmedrs757563721
geneviewrs757563721
scholarrs757563721
googlers757563721
pharmgkbrs757563721
gwascentralrs757563721
openSNPrs757563721
23andMers757563721
23andMe allrs757563721
SNP Nexus

SNPshotrs757563721
SNPdbers757563721
MSV3drs757563721
GWAS Ctlgrs757563721
Max Magnitude0
ClinVar
Risk rs757563721(T;T)
Alt rs757563721(T;T)
Reference rs757563721(G;G)
Significance Pathogenic
Disease Charcot-Marie-Tooth disease
Variation info
Gene MTMR2
CLNDBN Charcot-Marie-Tooth disease, type IV
Reversed 0
HGVS NC_000011.9:g.95582999G>A
CLNSRC
CLNACC RCV000228911.1,