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rs281865134

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs281865134(C;G)
Make rs281865134(G;G)
ReferenceGRCh38 38.1/141
Chromosome16
Position11553578
GeneLITAF
is asnp
is mentioned by
dbSNPrs281865134
ebirs281865134
HLIrs281865134
Exacrs281865134
Varsomers281865134
Maprs281865134
PheGenIrs281865134
hapmaprs281865134
1000 genomesrs281865134
hgdprs281865134
ensemblrs281865134
gopubmedrs281865134
geneviewrs281865134
scholarrs281865134
googlers281865134
pharmgkbrs281865134
gwascentralrs281865134
openSNPrs281865134
23andMers281865134
23andMe allrs281865134
SNP Nexus

SNPshotrs281865134
SNPdbers281865134
MSV3drs281865134
GWAS Ctlgrs281865134
Max Magnitude0
ClinVar
Risk rs281865134(G;G)
Alt rs281865134(G;G)
Reference rs281865134(C;C)
Significance Pathogenic
Disease Charcot-Marie-Tooth disease
Variation info
Gene LITAF
CLNDBN Charcot-Marie-Tooth disease, type 1C
Reversed 1
HGVS NC_000016.9:g.11647434G>C
CLNSRC ClinVar GeneReviews
CLNACC RCV000034128.2,