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rs587777715

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs587777715(A;T)
Make rs587777715(T;T)
ReferenceGRCh38 38.1/142
Chromosome6
Position109727107
GeneFIG4
is asnp
is mentioned by
dbSNPrs587777715
ebirs587777715
HLIrs587777715
Exacrs587777715
Varsomers587777715
Maprs587777715
PheGenIrs587777715
hapmaprs587777715
1000 genomesrs587777715
hgdprs587777715
ensemblrs587777715
gopubmedrs587777715
geneviewrs587777715
scholarrs587777715
googlers587777715
pharmgkbrs587777715
gwascentralrs587777715
openSNPrs587777715
23andMers587777715
23andMe allrs587777715
SNP Nexus

SNPshotrs587777715
SNPdbers587777715
MSV3drs587777715
GWAS Ctlgrs587777715
Max Magnitude0
ClinVar
Risk rs587777715(T;T)
Alt rs587777715(T;T)
Reference rs587777715(A;A)
Significance Pathogenic
Disease Charcot-Marie-Tooth disease
Variation info
Gene FIG4
CLNDBN Charcot-Marie-Tooth disease, type 4J
Reversed 0
HGVS NC_000006.11:g.110048310A>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000144073.3,