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rs6140226

From SNPedia

Orientationplus
Stabilizedplus
Make rs6140226(C;C)
Make rs6140226(C;T)
Make rs6140226(T;T)
ReferenceGRCh38 38.1/141
Chromosome20
Position7245836
GeneLOC101929265
is asnp
is mentioned by
dbSNPrs6140226
ebirs6140226
HLIrs6140226
Exacrs6140226
Varsomers6140226
Maprs6140226
PheGenIrs6140226
hapmaprs6140226
1000 genomesrs6140226
hgdprs6140226
ensemblrs6140226
gopubmedrs6140226
geneviewrs6140226
scholarrs6140226
googlers6140226
pharmgkbrs6140226
gwascentralrs6140226
openSNPrs6140226
23andMers6140226
23andMe allrs6140226
SNP Nexus

SNPshotrs6140226
SNPdbers6140226
MSV3drs6140226
GWAS Ctlgrs6140226
GMAF0.4238
Max Magnitude
? (C;C) (C;T) (T;T) 28
[PMID 23160099OA-icon.png] A genome-wide association study identifies susceptibility loci for nonsyndromic sagittal craniosynostosis near BMP2 and within BBS9


[PMID 17186469OA-icon.png] Mutations in the gene encoding the Wnt-signaling component R-spondin 4 (RSPO4) cause autosomal recessive anonychia.