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rs587776527

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 7 Fanconi anemia, complementation group N
(A;G) 3 2-4 fold higher risk for breast cancer, depending on family history
(G;G) 0 common in clinvar
ReferenceGRCh38.p2 38.2/144
Chromosome16
Position23607958
GenePALB2
is asnp
is mentioned by
dbSNPrs587776527
ebirs587776527
HLIrs587776527
Exacrs587776527
Varsomers587776527
Maprs587776527
PheGenIrs587776527
hapmaprs587776527
1000 genomesrs587776527
hgdprs587776527
ensemblrs587776527
gopubmedrs587776527
geneviewrs587776527
scholarrs587776527
googlers587776527
pharmgkbrs587776527
gwascentralrs587776527
openSNPrs587776527
23andMers587776527
23andMe allrs587776527
SNP Nexus

SNPshotrs587776527
SNPdbers587776527
MSV3drs587776527
GWAS Ctlgrs587776527
Max Magnitude7
ClinVar
Risk rs587776527(A;A)
Alt rs587776527(A;A)
Reference rs587776527(G;G)
Significance Other
Disease Pancreatic cancer 3 Hereditary cancer-predisposing syndrome Familial cancer of breast not provided
Variation info
Gene PALB2
CLNDBN Pancreatic cancer 3 Hereditary cancer-predisposing syndrome Familial cancer of breast not provided
Reversed 0
HGVS NC_000016.9:g.23619279G>A
CLNSRC OMIM Allelic Variant PALB2 database
CLNACC RCV000114612.3, RCV000160853.3, RCV000168017.2, RCV000212825.1,