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rs11696257

From SNPedia

Orientationplus
Stabilizedplus
Make rs11696257(C;C)
Make rs11696257(C;T)
Make rs11696257(T;T)
ReferenceGRCh38 38.1/141
Chromosome20
Position40642176
is asnp
is mentioned by
dbSNPrs11696257
ebirs11696257
HLIrs11696257
Exacrs11696257
Varsomers11696257
Maprs11696257
PheGenIrs11696257
hapmaprs11696257
1000 genomesrs11696257
hgdprs11696257
ensemblrs11696257
gopubmedrs11696257
geneviewrs11696257
scholarrs11696257
googlers11696257
pharmgkbrs11696257
gwascentralrs11696257
openSNPrs11696257
23andMers11696257
23andMe allrs11696257
SNP Nexus

SNPshotrs11696257
SNPdbers11696257
MSV3drs11696257
GWAS Ctlgrs11696257
Max Magnitude
? (C;C) (C;T) (T;T) 28

[PMID 24972815] Association study of single nucleotide polymorphisms of MAFB with non-syndromic cleft lip with or without cleft palate in a population in Heilongjiang Province, northern China


[PMID 26586245] Polymorphic variants near 1p22 and 20q11.2 loci and the risk of non-syndromic cleft lip and palate in South Indian population