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rs587776416

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(-;-) 7 Fanconi anemia, complementation group N
(-;AT) 3 significantly increased risk of breast cancer
(AT;AT) 0 common in clinvar
ReferenceGRCh38 38.1/142
Chromosome16
Position23629986
GenePALB2
is asnp
is mentioned by
dbSNPrs587776416
ebirs587776416
HLIrs587776416
Exacrs587776416
Varsomers587776416
Maprs587776416
PheGenIrs587776416
hapmaprs587776416
1000 genomesrs587776416
hgdprs587776416
ensemblrs587776416
gopubmedrs587776416
geneviewrs587776416
scholarrs587776416
googlers587776416
pharmgkbrs587776416
gwascentralrs587776416
openSNPrs587776416
23andMers587776416
23andMe allrs587776416
SNP Nexus

SNPshotrs587776416
SNPdbers587776416
MSV3drs587776416
GWAS Ctlgrs587776416
Max Magnitude7
ClinVar
Risk
Alt
Reference Rs587776416(AT;AT)
Significance Pathogenic
Disease Familial cancer of breast Hereditary cancer-predisposing syndrome not provided
Variation info
Gene PALB2
CLNDBN Familial cancer of breast Hereditary cancer-predisposing syndrome not provided
Reversed 1
HGVS NC_000016.9:g.23641307_23641308delAT
CLNSRC Ambry Genetics ClinVar
CLNACC RCV000123337.3, RCV000129400.4, RCV000133478.3,