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rs730881865

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(-;-) 7 Fanconi anemia, complementation group N
(-;A) 3 2-4 fold higher risk for breast cancer, depending on family history
(A;A) 0 common in clinvar
ReferenceGRCh38.p2 38.2/144
Chromosome16
Position23630230
GenePALB2
is asnp
is mentioned by
dbSNPrs730881865
ebirs730881865
HLIrs730881865
Exacrs730881865
Varsomers730881865
Maprs730881865
PheGenIrs730881865
hapmaprs730881865
1000 genomesrs730881865
hgdprs730881865
ensemblrs730881865
gopubmedrs730881865
geneviewrs730881865
scholarrs730881865
googlers730881865
pharmgkbrs730881865
gwascentralrs730881865
openSNPrs730881865
23andMers730881865
23andMe allrs730881865
SNP Nexus

SNPshotrs730881865
SNPdbers730881865
MSV3drs730881865
GWAS Ctlgrs730881865
Max Magnitude7
ClinVar
Risk rs730881865(;)
Alt rs730881865(;)
Reference rs730881865(A;A)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome not provided
Variation info
Gene PALB2
CLNDBN Hereditary cancer-predisposing syndrome not provided
Reversed 1
HGVS NC_000016.9:g.23641551delT
CLNSRC
CLNACC RCV000160805.3, RCV000212803.1,