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rs587777883

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587777883(G;T)
Make rs587777883(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome1
Position10303459
GeneKIF1B
is asnp
is mentioned by
dbSNPrs587777883
ebirs587777883
HLIrs587777883
Exacrs587777883
Varsomers587777883
Maprs587777883
PheGenIrs587777883
hapmaprs587777883
1000 genomesrs587777883
hgdprs587777883
ensemblrs587777883
gopubmedrs587777883
geneviewrs587777883
scholarrs587777883
googlers587777883
pharmgkbrs587777883
gwascentralrs587777883
openSNPrs587777883
23andMers587777883
23andMe allrs587777883
SNP Nexus

SNPshotrs587777883
SNPdbers587777883
MSV3drs587777883
GWAS Ctlgrs587777883
Max Magnitude0
ClinVar
Risk rs587777883(T;T)
Alt rs587777883(T;T)
Reference rs587777883(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene KIF1B
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.10363517G>T
CLNSRC
CLNACC RCV000143826.1,