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rs51526122

From SNPedia

Orientationplus
Stabilizedplus
Make rs51526122(A;A)
Make rs51526122(A;G)
Make rs51526122(G;G)
ReferenceGRCm38.p1 38.2/138
Chromosome5
Position56546164
is asnp
is mentioned by
dbSNPrs51526122
ebirs51526122
HLIrs51526122
Exacrs51526122
Varsomers51526122
Maprs51526122
PheGenIrs51526122
hapmaprs51526122
1000 genomesrs51526122
hgdprs51526122
ensemblrs51526122
gopubmedrs51526122
geneviewrs51526122
scholarrs51526122
googlers51526122
pharmgkbrs51526122
gwascentralrs51526122
openSNPrs51526122
23andMers51526122
23andMe allrs51526122
SNP Nexus

SNPshotrs51526122
SNPdbers51526122
MSV3drs51526122
GWAS Ctlgrs51526122
Max Magnitude
[PMID 25099575] Breast-Cancer Risk in Families with Mutations in PALB2

see also ClinVar (where clinical significance = pathogenic)