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rs6428370

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common/normal
Make rs6428370(A;G)
Make rs6428370(G;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position196875463
GeneLOC100289145
is asnp
is mentioned by
dbSNPrs6428370
ebirs6428370
HLIrs6428370
Exacrs6428370
Varsomers6428370
Maprs6428370
PheGenIrs6428370
hapmaprs6428370
1000 genomesrs6428370
hgdprs6428370
ensemblrs6428370
gopubmedrs6428370
geneviewrs6428370
scholarrs6428370
googlers6428370
pharmgkbrs6428370
gwascentralrs6428370
openSNPrs6428370
23andMers6428370
23andMe allrs6428370
SNP Nexus

SNPshotrs6428370
SNPdbers6428370
MSV3drs6428370
GWAS Ctlgrs6428370
GMAF0.3402
Max Magnitude0
? (A;A) (A;G) (G;G) 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 G
P-val 0.000007
Odds Ratio 1.43 [1.20-1.60]


GET Evidence
rs6428370
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.452381
summary