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

rs690347

From SNPedia

Orientationplus
Stabilizedplus
Make rs690347(G;G)
Make rs690347(G;T)
Make rs690347(T;T)
ReferenceGRCh38 38.1/141
Chromosome15
Position40813728
GeneZFYVE19
is asnp
is mentioned by
dbSNPrs690347
ebirs690347
HLIrs690347
Exacrs690347
Varsomers690347
Maprs690347
PheGenIrs690347
hapmaprs690347
1000 genomesrs690347
hgdprs690347
ensemblrs690347
gopubmedrs690347
geneviewrs690347
scholarrs690347
googlers690347
pharmgkbrs690347
gwascentralrs690347
openSNPrs690347
23andMers690347
23andMe allrs690347
SNP Nexus

SNPshotrs690347
SNPdbers690347
MSV3drs690347
GWAS Ctlgrs690347
GMAF0.1841
Max Magnitude
? (G;G) (G;T) (T;T) 28
Venter snp
Source plos
Gene ZFYVE19
allele G
frequency 0.84
sift TOLERATED
HuRef 1103645593857
Disease Association A chromosomal aberration involving ZFYVE19 is associated with acute myeloblastic leukemia (AML). Translocation t(11;15)(q23;q14) with MLL/HRX.



GET Evidence
ZFYVE19-S376A
aa_change Ser376Ala
aa_change_short S376A
impact not reviewed
qualified_impact Insufficiently evaluated not reviewed
overall_frequency 0.752041
summary