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rs863225023

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs863225023(C;T)
Make rs863225023(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome7
Position76304078
GeneHSPB1
is asnp
is mentioned by
dbSNPrs863225023
ebirs863225023
HLIrs863225023
Exacrs863225023
Varsomers863225023
Maprs863225023
PheGenIrs863225023
hapmaprs863225023
1000 genomesrs863225023
hgdprs863225023
ensemblrs863225023
gopubmedrs863225023
geneviewrs863225023
scholarrs863225023
googlers863225023
pharmgkbrs863225023
gwascentralrs863225023
openSNPrs863225023
23andMers863225023
23andMe allrs863225023
SNP Nexus

SNPshotrs863225023
SNPdbers863225023
MSV3drs863225023
GWAS Ctlgrs863225023
Max Magnitude0
ClinVar
Risk rs863225023(T;T)
Alt rs863225023(T;T)
Reference rs863225023(C;C)
Significance Pathogenic
Disease Charcot-Marie-Tooth disease type 2F not provided
Variation info
Gene HSPB1
CLNDBN Charcot-Marie-Tooth disease type 2F not provided
Reversed 0
HGVS NC_000007.13:g.75933395C>T
CLNSRC Quest Diagnostics
CLNACC RCV000201127.1, RCV000236115.1,