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rs6717918

From SNPedia

Orientationplus
Stabilizedplus
Make rs6717918(C;C)
Make rs6717918(C;T)
Make rs6717918(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position232290400
GeneDIS3L2
is asnp
is mentioned by
dbSNPrs6717918
ebirs6717918
HLIrs6717918
Exacrs6717918
Varsomers6717918
Maprs6717918
PheGenIrs6717918
hapmaprs6717918
1000 genomesrs6717918
hgdprs6717918
ensemblrs6717918
gopubmedrs6717918
geneviewrs6717918
scholarrs6717918
googlers6717918
pharmgkbrs6717918
gwascentralrs6717918
openSNPrs6717918
23andMers6717918
23andMe allrs6717918
SNP Nexus

SNPshotrs6717918
SNPdbers6717918
MSV3drs6717918
GWAS Ctlgrs6717918
GMAF0.4683
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


GET Evidence
rs6717918
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.508197
summary