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rs786200949

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs786200949(C;T)
Make rs786200949(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position240788208
GeneKIF1A
is asnp
is mentioned by
dbSNPrs786200949
ebirs786200949
HLIrs786200949
Exacrs786200949
Varsomers786200949
Maprs786200949
PheGenIrs786200949
hapmaprs786200949
1000 genomesrs786200949
hgdprs786200949
ensemblrs786200949
gopubmedrs786200949
geneviewrs786200949
scholarrs786200949
googlers786200949
pharmgkbrs786200949
gwascentralrs786200949
openSNPrs786200949
23andMers786200949
23andMe allrs786200949
SNP Nexus

SNPshotrs786200949
SNPdbers786200949
MSV3drs786200949
GWAS Ctlgrs786200949
Max Magnitude0
ClinVar
Risk rs786200949(T;T)
Alt rs786200949(T;T)
Reference rs786200949(C;C)
Significance Pathogenic
Disease Hereditary spastic paraplegia
Variation info
Gene KIF1A
CLNDBN Hereditary spastic paraplegia
Reversed 1
HGVS NC_000002.11:g.241727625G>A
CLNSRC
CLNACC RCV000167867.1,