Have questions? Visit https://www.reddit.com/r/SNPedia

rs25651

From SNPedia

Orientationminus
Stabilizedminus
Make rs25651(A;A)
Make rs25651(A;G)
Make rs25651(G;G)
ReferenceGRCh38 38.1/141
Chromosome15
Position89792557
GeneANPEP
is asnp
is mentioned by
dbSNPrs25651
ebirs25651
HLIrs25651
Exacrs25651
Varsomers25651
Maprs25651
PheGenIrs25651
hapmaprs25651
1000 genomesrs25651
hgdprs25651
ensemblrs25651
gopubmedrs25651
geneviewrs25651
scholarrs25651
googlers25651
pharmgkbrs25651
gwascentralrs25651
openSNPrs25651
23andMers25651
23andMe allrs25651
SNP Nexus

SNPshotrs25651
SNPdbers25651
MSV3drs25651
GWAS Ctlgrs25651
GMAF0.3154
Max Magnitude
? (A;A) (A;G) (G;G) 28


Venter snp
Source plos
Gene ANPEP
allele T
frequency 0.288
sift TOLERATED
HuRef 1103645680856
Disease Association Defects in ANPEP may be a cause of various types of leukemia or lymphoma.



[PMID 18682748OA-icon.png] Analysis of 17,576 potentially functional SNPs in three case-control studies of myocardial infarction.


[PMID 21881118OA-icon.png] Genetic variants and susceptibility to neurological complications following West Nile virus infection.


GET Evidence
ANPEP-S752N
aa_change Ser752Asn
aa_change_short S752N
impact not reviewed
qualified_impact Insufficiently evaluated not reviewed
overall_frequency 0.379532
summary