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rs1338041

From SNPedia

Orientationminus
Make rs1338041(G;G)
Make rs1338041(G;T)
Make rs1338041(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome13
Position101406511
GeneNALCN
is asnp
is mentioned by
dbSNPrs1338041
ebirs1338041
HLIrs1338041
Exacrs1338041
Varsomers1338041
Maprs1338041
PheGenIrs1338041
hapmaprs1338041
1000 genomesrs1338041
hgdprs1338041
ensemblrs1338041
gopubmedrs1338041
geneviewrs1338041
scholarrs1338041
googlers1338041
pharmgkbrs1338041
gwascentralrs1338041
openSNPrs1338041
23andMers1338041
23andMe allrs1338041
SNP Nexus

SNPshotrs1338041
SNPdbers1338041
MSV3drs1338041
GWAS Ctlgrs1338041
Max Magnitude
? (G;G) (G;T) (T;T) 28

[PMID 25256078] Lack of validation of variants associated with cervical dystonia risk: a GWAS replication study