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rs786203057

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(-;-) 7 Fanconi anemia, complementation group N
(-;AG) 3 2-4 fold higher risk for breast cancer, depending on family history
(AG;AG) 0 common in clinvar
ReferenceGRCh38.p2 38.2/146
Chromosome16
Position23635254
GenePALB2
is asnp
is mentioned by
dbSNPrs786203057
ebirs786203057
HLIrs786203057
Exacrs786203057
Varsomers786203057
Maprs786203057
PheGenIrs786203057
hapmaprs786203057
1000 genomesrs786203057
hgdprs786203057
ensemblrs786203057
gopubmedrs786203057
geneviewrs786203057
scholarrs786203057
googlers786203057
pharmgkbrs786203057
gwascentralrs786203057
openSNPrs786203057
23andMers786203057
23andMe allrs786203057
SNP Nexus

SNPshotrs786203057
SNPdbers786203057
MSV3drs786203057
GWAS Ctlgrs786203057
Max Magnitude7
ClinVar
Risk rs786203057(;)
Alt rs786203057(;)
Reference rs786203057(AG;AG)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene PALB2
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000016.9:g.23646575_23646576delCT
CLNSRC
CLNACC RCV000166194.1,