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rs4858847

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs4858847(C;T)
Make rs4858847(T;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position47657937
GeneSMARCC1
is asnp
is mentioned by
dbSNPrs4858847
ebirs4858847
HLIrs4858847
Exacrs4858847
Varsomers4858847
Maprs4858847
PheGenIrs4858847
hapmaprs4858847
1000 genomesrs4858847
hgdprs4858847
ensemblrs4858847
gopubmedrs4858847
geneviewrs4858847
scholarrs4858847
googlers4858847
pharmgkbrs4858847
gwascentralrs4858847
openSNPrs4858847
23andMers4858847
23andMe allrs4858847
SNP Nexus

SNPshotrs4858847
SNPdbers4858847
MSV3drs4858847
GWAS Ctlgrs4858847
Max Magnitude0
OMIM612278
DescINFLAMMATORY BOWEL DISEASE 19; IBD19
Variant
Relatedalso