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rs7554607

From SNPedia

Orientationplus
Stabilizedplus
Make rs7554607(A;A)
Make rs7554607(A;G)
Make rs7554607(G;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position237103303
GeneRYR2
is asnp
is mentioned by
dbSNPrs7554607
ebirs7554607
HLIrs7554607
Exacrs7554607
Varsomers7554607
Maprs7554607
PheGenIrs7554607
hapmaprs7554607
1000 genomesrs7554607
hgdprs7554607
ensemblrs7554607
gopubmedrs7554607
geneviewrs7554607
scholarrs7554607
googlers7554607
pharmgkbrs7554607
gwascentralrs7554607
openSNPrs7554607
23andMers7554607
23andMe allrs7554607
SNP Nexus

SNPshotrs7554607
SNPdbers7554607
MSV3drs7554607
GWAS Ctlgrs7554607
GMAF0.3659
Max Magnitude
? (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 A
P-val 0.000002
Odds Ratio 1.49 [1.20-1.70]


GET Evidence
rs7554607
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.41129
summary