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rs587777838

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs587777838(-;-)
Make rs587777838(-;A)
ReferenceGRCh38 38.1/142
Chromosome4
Position153315998
GeneTRIM2
is asnp
is mentioned by
dbSNPrs587777838
ebirs587777838
HLIrs587777838
Exacrs587777838
Varsomers587777838
Maprs587777838
PheGenIrs587777838
hapmaprs587777838
1000 genomesrs587777838
hgdprs587777838
ensemblrs587777838
gopubmedrs587777838
geneviewrs587777838
scholarrs587777838
googlers587777838
pharmgkbrs587777838
gwascentralrs587777838
openSNPrs587777838
23andMers587777838
23andMe allrs587777838
SNP Nexus

SNPshotrs587777838
SNPdbers587777838
MSV3drs587777838
GWAS Ctlgrs587777838
Max Magnitude0
ClinVar
Risk rs587777838(;)
Alt rs587777838(;)
Reference rs587777838(A;A)
Significance Pathogenic
Disease Charcot-Marie-Tooth disease
Variation info
Gene TRIM2
CLNDBN Charcot-Marie-Tooth disease, axonal, type 2R
Reversed 0
HGVS NC_000004.11:g.154237150delA
CLNSRC OMIM Allelic Variant
CLNACC RCV000074303.4,