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rs10488360

From SNPedia

Orientationplus
Stabilizedplus
Make rs10488360(A;A)
Make rs10488360(A;G)
Make rs10488360(G;G)
ReferenceGRCh38 38.1/141
Chromosome7
Position4371578
is asnp
is mentioned by
dbSNPrs10488360
ebirs10488360
HLIrs10488360
Exacrs10488360
Varsomers10488360
Maprs10488360
PheGenIrs10488360
hapmaprs10488360
1000 genomesrs10488360
hgdprs10488360
ensemblrs10488360
gopubmedrs10488360
geneviewrs10488360
scholarrs10488360
googlers10488360
pharmgkbrs10488360
gwascentralrs10488360
openSNPrs10488360
23andMers10488360
23andMe allrs10488360
SNP Nexus

SNPshotrs10488360
SNPdbers10488360
MSV3drs10488360
GWAS Ctlgrs10488360
GMAF0.3618
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS
SNP rs10488360
PubMedID [PMID 17903294OA-icon.png]
Condition Factor VII
Gene Intergenic
Risk Allele
pValue 7.00E-006
OR NA
95% CI



GET Evidence
rs10488360
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.367188
summary