Rs1376877

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Orientationplus
Make rs1376877(C;C)
Make rs1376877(C;T)
Make rs1376877(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position203407367
GeneABI2
is asnp
is mentioned by
dbSNPrs1376877
Exacrs1376877
PheGenIrs1376877
nextbiors1376877
hapmaprs1376877
1000 genomesrs1376877
hgdprs1376877
ensemblrs1376877
gopubmedrs1376877
geneviewrs1376877
scholarrs1376877
googlers1376877
pharmgkbrs1376877
gwascentralrs1376877
openSNPrs1376877
23andMers1376877
23andMe allrs1376877
SNP Nexus

SNPshotrs1376877
SNPdbers1376877
MSV3drs1376877
GMAF0.3829
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS
SNP rs1376877
PubMedID [PMID 17903303OA-icon.png]
Condition Other subclinical atherosclerosis traits
Gene ABI2
Risk Allele
pValue 4.00E-007
OR NA
95% CI



GET Evidence
rs1376877
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.429688
summary