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rs121908162

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121908162(C;T)
Make rs121908162(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position10324838
GeneKIF1B
is asnp
is mentioned by
dbSNPrs121908162
ebirs121908162
HLIrs121908162
Exacrs121908162
Varsomers121908162
Maprs121908162
PheGenIrs121908162
hapmaprs121908162
1000 genomesrs121908162
hgdprs121908162
ensemblrs121908162
gopubmedrs121908162
geneviewrs121908162
scholarrs121908162
googlers121908162
pharmgkbrs121908162
gwascentralrs121908162
openSNPrs121908162
23andMers121908162
23andMe allrs121908162
SNP Nexus

SNPshotrs121908162
SNPdbers121908162
MSV3drs121908162
GWAS Ctlgrs121908162
GMAF0.0009183
Max Magnitude0
OMIM605995
Desc
Variant0003
Relatedalso
ClinVar
Risk rs121908162(T;T)
Alt rs121908162(T;T)
Reference rs121908162(C;C)
Significance Other
Disease Neuroblastoma 1 Charcot-Marie-Tooth disease
Variation info
Gene KIF1B
CLNDBN Neuroblastoma 1 Charcot-Marie-Tooth disease, type 2
Reversed 0
HGVS NC_000001.10:g.10384896C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000004923.2, RCV000198737.1,