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rs11861007

From SNPedia

Orientationplus
Stabilizedplus
Make rs11861007(C;C)
Make rs11861007(C;T)
Make rs11861007(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome16
Position79204788
GeneMAF, WWOX
is asnp
is mentioned by
dbSNPrs11861007
dbSNP (old)rs11861007
ClinGenrs11861007
ebirs11861007
HLIrs11861007
Exacrs11861007
Gnomadrs11861007
Varsomers11861007
Maprs11861007
PheGenIrs11861007
Biobankrs11861007
1000 genomesrs11861007
hgdprs11861007
ensemblrs11861007
gopubmedrs11861007
geneviewrs11861007
scholarrs11861007
googlers11861007
pharmgkbrs11861007
gwascentralrs11861007
openSNPrs11861007
23andMers11861007
23andMe allrs11861007
SNPshotrs11861007
SNPdbers11861007
MSV3drs11861007
GWAS Ctlgrs11861007
Max Magnitude
? (C;C) (C;T) (T;T) 28

[PMID 29361163] Genomic and expression analyses identify a disease modifying variant for fibrostenotic Crohn's disease.