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rs180177090

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(-;-) 7 Fanconi anemia, complementation group N
(-;G) 3 increased risk of breast cancer
(G;G) 0 common in clinvar
ReferenceGRCh38 38.1/141
Chromosome16
Position23635849
GenePALB2
is asnp
is mentioned by
dbSNPrs180177090
ebirs180177090
HLIrs180177090
Exacrs180177090
Varsomers180177090
Maprs180177090
PheGenIrs180177090
hapmaprs180177090
1000 genomesrs180177090
hgdprs180177090
ensemblrs180177090
gopubmedrs180177090
geneviewrs180177090
scholarrs180177090
googlers180177090
pharmgkbrs180177090
gwascentralrs180177090
openSNPrs180177090
23andMers180177090
23andMe allrs180177090
SNP Nexus

SNPshotrs180177090
SNPdbers180177090
MSV3drs180177090
GWAS Ctlgrs180177090
Max Magnitude7
ClinVar
Risk rs180177090(;)
Alt rs180177090(;)
Reference rs180177090(G;G)
Significance Pathogenic
Disease Familial cancer of breast
Variation info
Gene PALB2
CLNDBN Familial cancer of breast
Reversed 1
HGVS NC_000016.9:g.23647170delC
CLNSRC PALB2 database
CLNACC RCV000114653.2,


[PMID 19333784] PALB2 sequence variants in young South African breast cancer patients.