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rs3803185

From SNPedia

Orientationminus
Stabilizedminus
Make rs3803185(A;A)
Make rs3803185(A;G)
Make rs3803185(G;G)
ReferenceGRCh38 38.1/141
Chromosome13
Position49630889
GeneARL11
is asnp
is mentioned by
dbSNPrs3803185
ebirs3803185
HLIrs3803185
Exacrs3803185
Varsomers3803185
Maprs3803185
PheGenIrs3803185
hapmaprs3803185
1000 genomesrs3803185
hgdprs3803185
ensemblrs3803185
gopubmedrs3803185
geneviewrs3803185
scholarrs3803185
googlers3803185
pharmgkbrs3803185
gwascentralrs3803185
openSNPrs3803185
23andMers3803185
23andMe allrs3803185
SNP Nexus

SNPshotrs3803185
SNPdbers3803185
MSV3drs3803185
GWAS Ctlgrs3803185
GMAF0.3081
Max Magnitude
? (A;A) (A;G) (G;G) 28
Venter snp
Source plos
Gene ARL11
allele C
frequency 0.467
sift TOLERATED
HuRef 1103649222084
Disease Association Defects in ARL11 may be a cause of susceptibility to chronic lymphocytic leukemia (CLL) (MIM:151400).



GET Evidence
ARL11-C148R
aa_change Cys148Arg
aa_change_short C148R
impact not reviewed
qualified_impact Insufficiently evaluated not reviewed
overall_frequency 0.384322
summary