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rs10493485

From SNPedia

Orientationplus
Stabilizedplus
Make rs10493485(A;A)
Make rs10493485(A;T)
Make rs10493485(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position71605446
GeneNEGR1
is asnp
is mentioned by
dbSNPrs10493485
ebirs10493485
HLIrs10493485
Exacrs10493485
Varsomers10493485
Maprs10493485
PheGenIrs10493485
hapmaprs10493485
1000 genomesrs10493485
hgdprs10493485
ensemblrs10493485
gopubmedrs10493485
geneviewrs10493485
scholarrs10493485
googlers10493485
pharmgkbrs10493485
gwascentralrs10493485
openSNPrs10493485
23andMers10493485
23andMe allrs10493485
SNP Nexus

SNPshotrs10493485
SNPdbers10493485
MSV3drs10493485
GWAS Ctlgrs10493485
GMAF0.3131
Max Magnitude
? (A;A) (A;T) (T;T) 28
GWAS
SNP rs10493485
PubMedID [PMID 17903294OA-icon.png]
Condition Hemostatic factors and hematological phenotypes
Gene NEGR1
Risk Allele
pValue 2.00E-006
OR NA
95% CI



GET Evidence
rs10493485
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.222222
summary