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rs10490113

From SNPedia

Orientationplus
Stabilizedplus
Make rs10490113(A;A)
Make rs10490113(A;C)
Make rs10490113(C;C)
ReferenceGRCh38 38.1/141
Chromosome2
Position59272212
GeneAC007131.1
is asnp
is mentioned by
dbSNPrs10490113
ebirs10490113
HLIrs10490113
Exacrs10490113
Varsomers10490113
Maprs10490113
PheGenIrs10490113
hapmaprs10490113
1000 genomesrs10490113
hgdprs10490113
ensemblrs10490113
gopubmedrs10490113
geneviewrs10490113
scholarrs10490113
googlers10490113
pharmgkbrs10490113
gwascentralrs10490113
openSNPrs10490113
23andMers10490113
23andMe allrs10490113
SNP Nexus

SNPshotrs10490113
SNPdbers10490113
MSV3drs10490113
GWAS Ctlgrs10490113
GMAF0.09596
Max Magnitude
? (A;A) (A;C) (C;C) 28
GWAS snp
PMID [PMID 17903305OA-icon.png]
Trait Breast cancer
Title A genome-wide association study of breast and prostate cancer in the NHLBI's Framingham Heart Study
Risk Allele
P-val 0.0000050000000000000004
Odds Ratio NR NR


GET Evidence
rs10490113
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.078125
summary