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rs6718438

From SNPedia

Orientationplus
Stabilizedplus
Make rs6718438(C;C)
Make rs6718438(C;T)
Make rs6718438(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position232290856
GeneDIS3L2
is asnp
is mentioned by
dbSNPrs6718438
ebirs6718438
HLIrs6718438
Exacrs6718438
Varsomers6718438
Maprs6718438
PheGenIrs6718438
hapmaprs6718438
1000 genomesrs6718438
hgdprs6718438
ensemblrs6718438
gopubmedrs6718438
geneviewrs6718438
scholarrs6718438
googlers6718438
pharmgkbrs6718438
gwascentralrs6718438
openSNPrs6718438
23andMers6718438
23andMe allrs6718438
SNP Nexus

SNPshotrs6718438
SNPdbers6718438
MSV3drs6718438
GWAS Ctlgrs6718438
GMAF0.4022
Max Magnitude
? (C;C) (C;T) (T;T) 28
[PMID 19570815OA-icon.png] A genome-wide association study of northwestern Europeans involves the CNP signaling pathway in the etiology of human height variation
OMIM613440
Desc
Variant
Relatedalso