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rs756660214

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
(-;-) 0 common/normal
(-;A) 3 2-4 fold higher risk for breast cancer, depending on family history
(A;A) 7 Fanconi anemia, complementation group N
ReferenceGRCh38.p2 38.2/144
Chromosome16
Position23635787
GenePALB2
is asnp
is mentioned by
dbSNPrs756660214
ebirs756660214
HLIrs756660214
Exacrs756660214
Varsomers756660214
Maprs756660214
PheGenIrs756660214
hapmaprs756660214
1000 genomesrs756660214
hgdprs756660214
ensemblrs756660214
gopubmedrs756660214
geneviewrs756660214
scholarrs756660214
googlers756660214
pharmgkbrs756660214
gwascentralrs756660214
openSNPrs756660214
23andMers756660214
23andMe allrs756660214
SNP Nexus

SNPshotrs756660214
SNPdbers756660214
MSV3drs756660214
GWAS Ctlgrs756660214
Max Magnitude7
ClinVar
Risk rs756660214(A;A)
Alt rs756660214(A;A)
Reference rs756660214(;)
Significance Other
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 0
HGVS NC_000016.9:g.23647109dupA
CLNSRC PALB2 database
CLNACC RCV000114661.5, RCV000129208.3, RCV000212780.1,