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rs751415161

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;-) 7 Fanconi anemia, complementation group N
(-;AAGT) 3 2-4 fold higher risk for breast cancer, depending on family history
(AAGT;AAGT) 0 common in clinvar
ReferenceGRCh38.p2 38.2/144
Chromosome16
Position23603591
GenePALB2
is asnp
is mentioned by
dbSNPrs751415161
ebirs751415161
HLIrs751415161
Exacrs751415161
Varsomers751415161
Maprs751415161
PheGenIrs751415161
hapmaprs751415161
1000 genomesrs751415161
hgdprs751415161
ensemblrs751415161
gopubmedrs751415161
geneviewrs751415161
scholarrs751415161
googlers751415161
pharmgkbrs751415161
gwascentralrs751415161
openSNPrs751415161
23andMers751415161
23andMe allrs751415161
SNP Nexus

SNPshotrs751415161
SNPdbers751415161
MSV3drs751415161
GWAS Ctlgrs751415161
Max Magnitude7
ClinVar
Risk rs751415161(;)
Alt rs751415161(;)
Reference rs751415161(AAGT;AAGT)
Significance Pathogenic
Disease not provided Hereditary cancer-predisposing syndrome
Variation info
Gene PALB2
CLNDBN not provided Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000016.9:g.23614912_23614915delAAGT
CLNSRC
CLNACC RCV000133486.1, RCV000165289.1,