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rs12059277

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs12059277(C;C)
Make rs12059277(C;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position160949838
GeneITLN2, RP11-544M22.1
is asnp
is mentioned by
dbSNPrs12059277
ebirs12059277
HLIrs12059277
Exacrs12059277
Varsomers12059277
Maprs12059277
PheGenIrs12059277
hapmaprs12059277
1000 genomesrs12059277
hgdprs12059277
ensemblrs12059277
gopubmedrs12059277
geneviewrs12059277
scholarrs12059277
googlers12059277
pharmgkbrs12059277
gwascentralrs12059277
openSNPrs12059277
23andMers12059277
23andMe allrs12059277
SNP Nexus

SNPshotrs12059277
SNPdbers12059277
MSV3drs12059277
GWAS Ctlgrs12059277
GMAF0.02984
Max Magnitude0
? (C;C) (C;G) (G;G) 28
OMIM271665
DescSPONDYLOMETAEPIPHYSEAL DYSPLASIA, SHORT LIMB-HAND TYPE
Variant
Relatedalso