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rs78950893

From SNPedia

Orientationplus
Make rs78950893(C;C)
Make rs78950893(C;T)
Make rs78950893(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome18
Position48942348
GeneSMAD7
is asnp
is mentioned by
dbSNPrs78950893
ebirs78950893
HLIrs78950893
Exacrs78950893
Varsomers78950893
Maprs78950893
PheGenIrs78950893
hapmaprs78950893
1000 genomesrs78950893
hgdprs78950893
ensemblrs78950893
gopubmedrs78950893
geneviewrs78950893
scholarrs78950893
googlers78950893
pharmgkbrs78950893
gwascentralrs78950893
openSNPrs78950893
23andMers78950893
23andMe allrs78950893
SNP Nexus

SNPshotrs78950893
SNPdbers78950893
MSV3drs78950893
GWAS Ctlgrs78950893
Max Magnitude

[PMID 27242896] Fine-Mapping of 18q21.1 Locus Identifies Single Nucleotide Polymorphisms Associated with Nonsyndromic Cleft Lip with or without Cleft Palate.