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rs10518765

From SNPedia

Orientationplus
Stabilizedplus
Make rs10518765(A;A)
Make rs10518765(A;C)
Make rs10518765(C;C)
ReferenceGRCh38 38.1/141
Chromosome15
Position54388434
GeneUNC13C
is asnp
is mentioned by
dbSNPrs10518765
ebirs10518765
HLIrs10518765
Exacrs10518765
Varsomers10518765
Maprs10518765
PheGenIrs10518765
hapmaprs10518765
1000 genomesrs10518765
hgdprs10518765
ensemblrs10518765
gopubmedrs10518765
geneviewrs10518765
scholarrs10518765
googlers10518765
pharmgkbrs10518765
gwascentralrs10518765
openSNPrs10518765
23andMers10518765
23andMe allrs10518765
SNP Nexus

SNPshotrs10518765
SNPdbers10518765
MSV3drs10518765
GWAS Ctlgrs10518765
GMAF0.1387
Max Magnitude
? (A;A) (A;C) (C;C) 28
GWAS snp
PMID [PMID 17903293OA-icon.png]
Trait Select biomarker traits
Title Genome-wide association with select biomarker traits in the Framingham Heart Study
Risk Allele
P-val 9.9999999999999995E-7
Odds Ratio NR NR


[PMID 17052657] Genome-wide genotyping in Parkinson's disease and neurologically normal controls: first stage analysis and public release of data.


GET Evidence
rs10518765
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.0859375
summary