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rs1881797

From SNPedia

Orientationplus
Stabilizedplus
Make rs1881797(C;C)
Make rs1881797(C;T)
Make rs1881797(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position247526230
GeneIGKV1D-17
is asnp
is mentioned by
dbSNPrs1881797
ebirs1881797
HLIrs1881797
Exacrs1881797
Varsomers1881797
Maprs1881797
PheGenIrs1881797
hapmaprs1881797
1000 genomesrs1881797
hgdprs1881797
ensemblrs1881797
gopubmedrs1881797
geneviewrs1881797
scholarrs1881797
googlers1881797
pharmgkbrs1881797
gwascentralrs1881797
openSNPrs1881797
23andMers1881797
23andMe allrs1881797
SNP Nexus

SNPshotrs1881797
SNPdbers1881797
MSV3drs1881797
GWAS Ctlgrs1881797
GMAF0.2374
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 19684603OA-icon.png]
Trait Acute lymphoblastic leukemia (childhood)
Title Germline genomic variants associated with childhood acute lymphoblastic leukemia
Risk Allele C
P-val 0.000007
Odds Ratio 1.52 [1.20-1.80]


GET Evidence
rs1881797
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.734375
summary