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rs515726122

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
(G;G) 0 common in clinvar
(G;T) 3 2-4 fold higher risk for breast cancer, depending on family history
(T;T) 7 Fanconi anemia, complementation group N
ReferenceGRCh38 38.1/142
Chromosome16
Position23636043
GenePALB2
is asnp
is mentioned by
dbSNPrs515726122
ebirs515726122
HLIrs515726122
Exacrs515726122
Varsomers515726122
Maprs515726122
PheGenIrs515726122
hapmaprs515726122
1000 genomesrs515726122
hgdprs515726122
ensemblrs515726122
gopubmedrs515726122
geneviewrs515726122
scholarrs515726122
googlers515726122
pharmgkbrs515726122
gwascentralrs515726122
openSNPrs515726122
23andMers515726122
23andMe allrs515726122
SNP Nexus

SNPshotrs515726122
SNPdbers515726122
MSV3drs515726122
GWAS Ctlgrs515726122
Max Magnitude7
ClinVar
Risk rs515726122(A,G,T;A,G,T)
Alt rs515726122(A,G,T;A,G,T)
Reference rs515726122(C;C)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome Familial cancer of breast
Variation info
Gene PALB2
CLNDBN Hereditary cancer-predisposing syndrome Familial cancer of breast
Reversed 1
HGVS NC_000016.9:g.23647364G>A; NC_000016.9:g.23647364G>T
CLNSRC PALB2 database
CLNACC RCV000166977.1, RCV000114642.1,