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rs1076165

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs1076165(A;A)
Make rs1076165(A;G)
ReferenceGRCh38 38.1/141
Chromosome17
Position2870106
GeneRAP1GAP2
is asnp
is mentioned by
dbSNPrs1076165
ebirs1076165
HLIrs1076165
Exacrs1076165
Varsomers1076165
Maprs1076165
PheGenIrs1076165
hapmaprs1076165
1000 genomesrs1076165
hgdprs1076165
ensemblrs1076165
gopubmedrs1076165
geneviewrs1076165
scholarrs1076165
googlers1076165
pharmgkbrs1076165
gwascentralrs1076165
openSNPrs1076165
23andMers1076165
23andMe allrs1076165
SNP Nexus

SNPshotrs1076165
SNPdbers1076165
MSV3drs1076165
GWAS Ctlgrs1076165
GMAF0.2222
Max Magnitude0
? (A;A) (A;G) (G;G) 28
OMIM612255
DescINFLAMMATORY BOWEL DISEASE 15; IBD15
Variant
Relatedalso