Have questions? Visit https://www.reddit.com/r/SNPedia

rs267606772

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs267606772(A;A)
Make rs267606772(A;G)
ReferenceGRCh38 38.1/141
Chromosome19
Position10793799
GeneDNM2
is asnp
is mentioned by
dbSNPrs267606772
ebirs267606772
HLIrs267606772
Exacrs267606772
Varsomers267606772
Maprs267606772
PheGenIrs267606772
hapmaprs267606772
1000 genomesrs267606772
hgdprs267606772
ensemblrs267606772
gopubmedrs267606772
geneviewrs267606772
scholarrs267606772
googlers267606772
pharmgkbrs267606772
gwascentralrs267606772
openSNPrs267606772
23andMers267606772
23andMe allrs267606772
SNP Nexus

SNPshotrs267606772
SNPdbers267606772
MSV3drs267606772
GWAS Ctlgrs267606772
Max Magnitude0
ClinVar
Risk rs267606772(A;A)
Alt rs267606772(A;A)
Reference rs267606772(G;G)
Significance Pathogenic
Disease Charcot-Marie-Tooth disease DNM2-related intermediate Charcot-Marie-Tooth neuropathy
Variation info
Gene DNM2
CLNDBN Charcot-Marie-Tooth disease, type 2M DNM2-related intermediate Charcot-Marie-Tooth neuropathy
Reversed 0
HGVS NC_000019.9:g.10904475G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000007710.2, RCV000203266.1,