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rs200561798

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs200561798(C;C)
Make rs200561798(C;T)
ReferenceGRCh38 38.1/142
Chromosome1
Position10361732
GeneKIF1B
is asnp
is mentioned by
dbSNPrs200561798
ebirs200561798
HLIrs200561798
Exacrs200561798
Varsomers200561798
Maprs200561798
PheGenIrs200561798
hapmaprs200561798
1000 genomesrs200561798
hgdprs200561798
ensemblrs200561798
gopubmedrs200561798
geneviewrs200561798
scholarrs200561798
googlers200561798
pharmgkbrs200561798
gwascentralrs200561798
openSNPrs200561798
23andMers200561798
23andMe allrs200561798
SNP Nexus

SNPshotrs200561798
SNPdbers200561798
MSV3drs200561798
GWAS Ctlgrs200561798
Max Magnitude0
ClinVar
Risk rs200561798(C;C)
Alt rs200561798(C;C)
Reference rs200561798(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene KIF1B
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.10421790T>C
CLNSRC ClinVar
CLNACC RCV000143821.1,