Rs897453

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Orientationminus
Make rs897453(A;A)
Make rs897453(A;G)
Make rs897453(G;G)
ReferenceGRCh38 38.1/141
Chromosome17
Position17522317
GenePEMT
is asnp
is mentioned by
dbSNPrs897453
Exacrs897453
PheGenIrs897453
nextbiors897453
hapmaprs897453
1000 genomesrs897453
hgdprs897453
ensemblrs897453
gopubmedrs897453
geneviewrs897453
scholarrs897453
googlers897453
pharmgkbrs897453
gwascentralrs897453
openSNPrs897453
23andMers897453
23andMe allrs897453
SNP Nexus

SNPshotrs897453
SNPdbers897453
MSV3drs897453
GMAF0.2466
? (A;A) (A;G) (G;G) 28


Venter snp
Source plos
Gene PEMT
allele G
frequency
sift TOLERATED
HuRef 1103645292897
Disease Association Deletion of PEMT may be related to liver cancer.



GET Evidence
PEMT-V95I
aa_change Val95Ile
aa_change_short V95I
impact not reviewed
qualified_impact Insufficiently evaluated not reviewed
overall_frequency 0.338632
summary