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rs10870077

From SNPedia

Orientationplus
Stabilizedplus
Make rs10870077(C;C)
Make rs10870077(C;G)
Make rs10870077(G;G)
ReferenceGRCh38 38.1/141
Chromosome9
Position136369439
GeneCARD9
is asnp
is mentioned by
dbSNPrs10870077
ebirs10870077
HLIrs10870077
Exacrs10870077
Varsomers10870077
Maprs10870077
PheGenIrs10870077
hapmaprs10870077
1000 genomesrs10870077
hgdprs10870077
ensemblrs10870077
gopubmedrs10870077
geneviewrs10870077
scholarrs10870077
googlers10870077
pharmgkbrs10870077
gwascentralrs10870077
openSNPrs10870077
23andMers10870077
23andMe allrs10870077
SNP Nexus

SNPshotrs10870077
SNPdbers10870077
MSV3drs10870077
GWAS Ctlgrs10870077
GMAF0.3641
Max Magnitude
? (C;C) (C;G) (G;G) 28
OMIM266600
DescINFLAMMATORY BOWEL DISEASE 1; IBD1
Variant
Relatedalso



GET Evidence
rs10870077
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.320312
summary