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rs7249222

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs7249222(A;A)
Make rs7249222(A;G)
ReferenceGRCh38 38.1/141
Chromosome19
Position41237956
GeneAXL
is asnp
is mentioned by
dbSNPrs7249222
ebirs7249222
HLIrs7249222
Exacrs7249222
Varsomers7249222
Maprs7249222
PheGenIrs7249222
hapmaprs7249222
1000 genomesrs7249222
hgdprs7249222
ensemblrs7249222
gopubmedrs7249222
geneviewrs7249222
scholarrs7249222
googlers7249222
pharmgkbrs7249222
gwascentralrs7249222
openSNPrs7249222
23andMers7249222
23andMe allrs7249222
SNP Nexus

SNPshotrs7249222
SNPdbers7249222
MSV3drs7249222
GWAS Ctlgrs7249222
GMAF0
Max Magnitude0
? (A;A) (A;G) (G;G) 28
Venter snp
Source plos
Gene AXL
allele G
frequency 1
sift TOLERATED
HuRef 1103691147228
Disease Association Has transforming potential in patients with chronic myeloproliferative disorder or chronic myelocytic leukemia.



GET Evidence
AXL-N266D
aa_change Asn266Asp
aa_change_short N266D
impact not reviewed
qualified_impact Insufficiently evaluated not reviewed
overall_frequency 1
summary