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rs797044848

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs797044848(C;G)
Make rs797044848(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome16
Position11549719
GeneLITAF
is asnp
is mentioned by
dbSNPrs797044848
ebirs797044848
HLIrs797044848
Exacrs797044848
Varsomers797044848
Maprs797044848
PheGenIrs797044848
hapmaprs797044848
1000 genomesrs797044848
hgdprs797044848
ensemblrs797044848
gopubmedrs797044848
geneviewrs797044848
scholarrs797044848
googlers797044848
pharmgkbrs797044848
gwascentralrs797044848
openSNPrs797044848
23andMers797044848
23andMe allrs797044848
SNP Nexus

SNPshotrs797044848
SNPdbers797044848
MSV3drs797044848
GWAS Ctlgrs797044848
Max Magnitude0
ClinVar
Risk rs797044848(G;G)
Alt rs797044848(G;G)
Reference rs797044848(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.11643575G>C
CLNSRC
CLNACC RCV000193485.1,