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rs281865063

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs281865063(A;A)
Make rs281865063(A;G)
ReferenceGRCh38 38.1/141
Chromosome12
Position32611270
GeneFGD4
is asnp
is mentioned by
dbSNPrs281865063
ebirs281865063
HLIrs281865063
Exacrs281865063
Varsomers281865063
Maprs281865063
PheGenIrs281865063
hapmaprs281865063
1000 genomesrs281865063
hgdprs281865063
ensemblrs281865063
gopubmedrs281865063
geneviewrs281865063
scholarrs281865063
googlers281865063
pharmgkbrs281865063
gwascentralrs281865063
openSNPrs281865063
23andMers281865063
23andMe allrs281865063
SNP Nexus

SNPshotrs281865063
SNPdbers281865063
MSV3drs281865063
GWAS Ctlgrs281865063
Max Magnitude0
ClinVar
Risk rs281865063(A;A)
Alt rs281865063(A;A)
Reference rs281865063(G;G)
Significance Pathogenic
Disease Charcot-Marie-Tooth disease
Variation info
Gene FGD4
CLNDBN Charcot-Marie-Tooth disease, type 4H
Reversed 0
HGVS NC_000012.11:g.32764204G>A
CLNSRC ClinVar GeneReviews
CLNACC RCV000031999.1,