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rs730881888

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 7 Fanconi anemia, complementation group N
(A;T) 3 2-4 fold higher risk for breast cancer, depending on family history
(T;T) 0 common in clinvar
ReferenceGRCh38.p2 38.2/144
Chromosome16
Position23629925
GenePALB2
is asnp
is mentioned by
dbSNPrs730881888
ebirs730881888
HLIrs730881888
Exacrs730881888
Varsomers730881888
Maprs730881888
PheGenIrs730881888
hapmaprs730881888
1000 genomesrs730881888
hgdprs730881888
ensemblrs730881888
gopubmedrs730881888
geneviewrs730881888
scholarrs730881888
googlers730881888
pharmgkbrs730881888
gwascentralrs730881888
openSNPrs730881888
23andMers730881888
23andMe allrs730881888
SNP Nexus

SNPshotrs730881888
SNPdbers730881888
MSV3drs730881888
GWAS Ctlgrs730881888
Max Magnitude7
ClinVar
Risk rs730881888(A;A)
Alt rs730881888(A;A)
Reference rs730881888(T;T)
Significance Pathogenic
Disease Familial cancer of breast Tumor susceptibility linked to germline BAP1 mutations not provided
Variation info
Gene PALB2
CLNDBN Familial cancer of breast Tumor susceptibility linked to germline BAP1 mutations not provided
Reversed 1
HGVS NC_000016.9:g.23641246A>G; NC_000016.9:g.23641246A>T
CLNSRC
CLNACC RCV000199909.1, RCV000219447.1, RCV000160839.2,