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rs797044847

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs797044847(A;A)
Make rs797044847(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome16
Position11549738
GeneLITAF
is asnp
is mentioned by
dbSNPrs797044847
ebirs797044847
HLIrs797044847
Exacrs797044847
Varsomers797044847
Maprs797044847
PheGenIrs797044847
hapmaprs797044847
1000 genomesrs797044847
hgdprs797044847
ensemblrs797044847
gopubmedrs797044847
geneviewrs797044847
scholarrs797044847
googlers797044847
pharmgkbrs797044847
gwascentralrs797044847
openSNPrs797044847
23andMers797044847
23andMe allrs797044847
SNP Nexus

SNPshotrs797044847
SNPdbers797044847
MSV3drs797044847
GWAS Ctlgrs797044847
Max Magnitude0
ClinVar
Risk rs797044847(A;A)
Alt rs797044847(A;A)
Reference rs797044847(G;G)
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.11643594C>T
CLNSRC
CLNACC RCV000192669.1,