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rs11646137

From SNPedia

Orientationplus
Stabilizedplus
Make rs11646137(C;C)
Make rs11646137(C;T)
Make rs11646137(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome16
Position3947029
is asnp
is mentioned by
dbSNPrs11646137
dbSNP (old)rs11646137
ClinGenrs11646137
ebirs11646137
HLIrs11646137
Exacrs11646137
Gnomadrs11646137
Varsomers11646137
Maprs11646137
PheGenIrs11646137
Biobankrs11646137
1000 genomesrs11646137
hgdprs11646137
ensemblrs11646137
gopubmedrs11646137
geneviewrs11646137
scholarrs11646137
googlers11646137
pharmgkbrs11646137
gwascentralrs11646137
openSNPrs11646137
23andMers11646137
23andMe allrs11646137
SNPshotrs11646137
SNPdbers11646137
MSV3drs11646137
GWAS Ctlgrs11646137
Max Magnitude
? (C;C) (C;T) (T;T) 28

[PMID 28402597OA-icon.png] Gene-gene interaction of single nucleotide polymorphisms in 16p13.3 may contribute to the risk of non-syndromic cleft lip with or without cleft palate in Chinese case-parent trios.