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rs762826555

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs762826555(A;A)
Make rs762826555(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome17
Position28739185
GeneNEK8
is asnp
is mentioned by
dbSNPrs762826555
ebirs762826555
HLIrs762826555
Exacrs762826555
Varsomers762826555
Maprs762826555
PheGenIrs762826555
hapmaprs762826555
1000 genomesrs762826555
hgdprs762826555
ensemblrs762826555
gopubmedrs762826555
geneviewrs762826555
scholarrs762826555
googlers762826555
pharmgkbrs762826555
gwascentralrs762826555
openSNPrs762826555
23andMers762826555
23andMe allrs762826555
SNP Nexus

SNPshotrs762826555
SNPdbers762826555
MSV3drs762826555
GWAS Ctlgrs762826555
Max Magnitude0
ClinVar
Risk rs762826555(A;A)
Alt rs762826555(A;A)
Reference rs762826555(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene NEK8
CLNDBN not provided
Reversed 0
HGVS NC_000017.10:g.27066203G>A
CLNSRC
CLNACC RCV000171252.1,