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rs587777108

From SNPedia

Orientationplus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
(T;T) 0 common in clinvar
Make rs587777108(C;C)
Make rs587777108(C;T)
ReferenceGRCh38 38.1/142
Chromosome11
Position63646550
GeneATL3
is asnp
is mentioned by
dbSNPrs587777108
ClinGenrs587777108
ebirs587777108
HLIrs587777108
Exacrs587777108
Varsomers587777108
Maprs587777108
PheGenIrs587777108
hapmaprs587777108
1000 genomesrs587777108
hgdprs587777108
ensemblrs587777108
gopubmedrs587777108
geneviewrs587777108
scholarrs587777108
googlers587777108
pharmgkbrs587777108
gwascentralrs587777108
openSNPrs587777108
23andMers587777108
23andMe allrs587777108
SNP Nexus

SNPshotrs587777108
SNPdbers587777108
MSV3drs587777108
GWAS Ctlgrs587777108
Max Magnitude0
ClinVar
Risk rs587777108(C;C) Rs587777108(T;T)
Alt rs587777108(C;C) Rs587777108(T;T)
Reference Rs587777108(A;A)
Significance Pathogenic
Disease Hereditary sensory neuropathy type IF
Variation info
Gene ATL3
CLNDBN Hereditary sensory neuropathy type IF
Reversed 1
HGVS NC_000011.9:g.63414022T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000083312.3,