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rs10787738

From SNPedia

Orientationplus
Stabilizedplus
Make rs10787738(C;C)
Make rs10787738(C;T)
Make rs10787738(T;T)
ReferenceGRCh38 38.1/142
Chromosome10
Position117017860
GeneSHTN1
is asnp
is mentioned by
dbSNPrs10787738
dbSNP (classic)rs10787738
ClinGenrs10787738
ebirs10787738
HLIrs10787738
Exacrs10787738
Gnomadrs10787738
Varsomers10787738
LitVarrs10787738
Maprs10787738
PheGenIrs10787738
Biobankrs10787738
1000 genomesrs10787738
hgdprs10787738
ensemblrs10787738
geneviewrs10787738
scholarrs10787738
googlers10787738
pharmgkbrs10787738
gwascentralrs10787738
openSNPrs10787738
23andMers10787738
SNPshotrs10787738
SNPdbers10787738
MSV3drs10787738
GWAS Ctlgrs10787738
Max Magnitude0
? (C;C) (C;T) (T;T) 28


[PMID 25099202] Genetic risk factors for orofacial clefts in Central Africans and Southeast Asians