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rs231591

From SNPedia

Orientationminus
Stabilizedminus
Make rs231591(C;C)
Make rs231591(C;T)
Make rs231591(T;T)
ReferenceGRCh38 38.1/141
Chromosome19
Position35733804
GeneKMT2B
is asnp
is mentioned by
dbSNPrs231591
ebirs231591
HLIrs231591
Exacrs231591
Varsomers231591
Maprs231591
PheGenIrs231591
hapmaprs231591
1000 genomesrs231591
hgdprs231591
ensemblrs231591
gopubmedrs231591
geneviewrs231591
scholarrs231591
googlers231591
pharmgkbrs231591
gwascentralrs231591
openSNPrs231591
23andMers231591
23andMe allrs231591
SNP Nexus

SNPshotrs231591
SNPdbers231591
MSV3drs231591
GWAS Ctlgrs231591
GMAF0.4362
Max Magnitude
? (C;C) (C;T) (T;T) 28


Venter snp
Source plos
Gene MLL4_HUMAN
allele G
frequency 0.466
sift
HuRef 1103691136789
Disease Association Often amplified in pancreatic carcinomas.



GET Evidence
NM_014727-D2361G
aa_change Asp2361Gly
aa_change_short D2361G
impact not reviewed
qualified_impact Insufficiently evaluated not reviewed
overall_frequency 0.57644
summary