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rs1057518379

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1057518379(C;C)
Make rs1057518379(C;T)
ReferenceGRCh38.p7 38.3/150
Chromosome14
Position75113369
GeneNEK9
is asnp
is mentioned by
dbSNPrs1057518379
dbSNP (old)rs1057518379
ClinGenrs1057518379
ebirs1057518379
HLIrs1057518379
Exacrs1057518379
Gnomadrs1057518379
Varsomers1057518379
LitVarrs1057518379
Maprs1057518379
PheGenIrs1057518379
Biobankrs1057518379
1000 genomesrs1057518379
hgdprs1057518379
ensemblrs1057518379
gopubmedrs1057518379
geneviewrs1057518379
scholarrs1057518379
googlers1057518379
pharmgkbrs1057518379
gwascentralrs1057518379
openSNPrs1057518379
23andMers1057518379
23andMe allrs1057518379
SNPshotrs1057518379
SNPdbers1057518379
MSV3drs1057518379
GWAS Ctlgrs1057518379
Max Magnitude0
ClinVar
Risk rs1057518379(C;C)
Alt rs1057518379(C;C)
Reference Rs1057518379(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene NEK9
CLNDBN not provided
Reversed 1
HGVS NC_000014.8:g.75580072A>G
CLNSRC
CLNACC RCV000414495.1,