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rs1064796397

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Chromosome15
Position40651562
GeneCASC5, KNL1
is asnp
is mentioned by
dbSNPrs1064796397
dbSNP (old)rs1064796397
ClinGenrs1064796397
ebirs1064796397
HLIrs1064796397
Exacrs1064796397
Gnomadrs1064796397
Varsomers1064796397
Maprs1064796397
PheGenIrs1064796397
Biobankrs1064796397
1000 genomesrs1064796397
hgdprs1064796397
ensemblrs1064796397
gopubmedrs1064796397
geneviewrs1064796397
scholarrs1064796397
googlers1064796397
pharmgkbrs1064796397
gwascentralrs1064796397
openSNPrs1064796397
23andMers1064796397
23andMe allrs1064796397
SNPshotrs1064796397
SNPdbers1064796397
MSV3drs1064796397
GWAS Ctlgrs1064796397
Max Magnitude0
ClinVar
Risk rs1064796397(-;-)
Alt rs1064796397(-;-)
Reference Rs1064796397(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene KNL1
CLNDBN not provided
Reversed 0
HGVS NC_000015.9:g.40943760delG
CLNSRC
CLNACC RCV000479917.1,