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rs765061840

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs765061840(A;A)
Make rs765061840(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome15
Position44633619
GeneSPG11
is asnp
is mentioned by
dbSNPrs765061840
ebirs765061840
HLIrs765061840
Exacrs765061840
Varsomers765061840
Maprs765061840
PheGenIrs765061840
hapmaprs765061840
1000 genomesrs765061840
hgdprs765061840
ensemblrs765061840
gopubmedrs765061840
geneviewrs765061840
scholarrs765061840
googlers765061840
pharmgkbrs765061840
gwascentralrs765061840
openSNPrs765061840
23andMers765061840
23andMe allrs765061840
SNP Nexus

SNPshotrs765061840
SNPdbers765061840
MSV3drs765061840
GWAS Ctlgrs765061840
Max Magnitude0
ClinVar
Risk rs765061840(A;A)
Alt rs765061840(A;A)
Reference rs765061840(G;G)
Significance Pathogenic
Disease Charcot-Marie-Tooth disease
Variation info
Gene SPG11
CLNDBN Charcot-Marie-Tooth disease, axonal type 2X
Reversed 0
HGVS NC_000015.9:g.44925817G>A
CLNSRC
CLNACC RCV000224985.1,