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rs9557635

From SNPedia

Orientationplus
Stabilizedplus
Make rs9557635(A;A)
Make rs9557635(A;G)
Make rs9557635(G;G)
ReferenceGRCh38 38.1/141
Chromosome13
Position101398739
GeneNALCN
is asnp
is mentioned by
dbSNPrs9557635
dbSNP (classic)rs9557635
ClinGenrs9557635
ebirs9557635
HLIrs9557635
Exacrs9557635
Gnomadrs9557635
Varsomers9557635
LitVarrs9557635
Maprs9557635
PheGenIrs9557635
Biobankrs9557635
1000 genomesrs9557635
hgdprs9557635
ensemblrs9557635
geneviewrs9557635
scholarrs9557635
googlers9557635
pharmgkbrs9557635
gwascentralrs9557635
openSNPrs9557635
23andMers9557635
SNPshotrs9557635
SNPdbers9557635
MSV3drs9557635
GWAS Ctlgrs9557635
GMAF0.2309
Max Magnitude0
? (A;A) (A;G) (G;G) 28


GWAS snp
PMID [PMID 23144319]
Trait Non-small cell lung cancer
Title Prognostic implications of genetic variants in advanced non-small cell lung cancer: a genome-wide association study.
Risk Allele A
P-val 9E-6
Odds Ratio NR NR