Rs104894519

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Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs104894519(A;A)
Make rs104894519(A;G)
ReferenceGRCh38 38.1/141
Chromosome16
Position11553576
GeneLITAF
is asnp
is mentioned by
dbSNPrs104894519
PheGenIrs104894519
nextbiors104894519
hapmaprs104894519
1000 genomesrs104894519
hgdprs104894519
ensemblrs104894519
gopubmedrs104894519
geneviewrs104894519
scholarrs104894519
googlers104894519
pharmgkbrs104894519
gwascentralrs104894519
openSNPrs104894519
23andMers104894519
23andMe allrs104894519
SNP Nexus

SNPshotrs104894519
SNPdbers104894519
MSV3drs104894519
Max Magnitude0
OMIM603795
Desc
Variant0001
Relatedalso
ClinVar
Risk rs104894519(A;A)
Alt rs104894519(A;A)
Reference rs104894519(G;G)
Significance Pathogenic
Disease Charcot-Marie-Tooth disease
Variation info
Gene LITAF
CLNDBN Charcot-Marie-Tooth disease, type IC
Reversed 1
HGVS NC_000016.9:g.11647432C>T
CLNSRC GeneReviews OMIM Allelic Variant
CLNACC RCV000006429.2,