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rs864622280

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs864622280(C;C)
Make rs864622280(C;G)
ReferenceGRCh38.p2 38.2/147
Chromosome16
Position23636005
GenePALB2
is asnp
is mentioned by
dbSNPrs864622280
ebirs864622280
HLIrs864622280
Exacrs864622280
Varsomers864622280
Maprs864622280
PheGenIrs864622280
hapmaprs864622280
1000 genomesrs864622280
hgdprs864622280
ensemblrs864622280
gopubmedrs864622280
geneviewrs864622280
scholarrs864622280
googlers864622280
pharmgkbrs864622280
gwascentralrs864622280
openSNPrs864622280
23andMers864622280
23andMe allrs864622280
SNP Nexus

SNPshotrs864622280
SNPdbers864622280
MSV3drs864622280
GWAS Ctlgrs864622280
Max Magnitude0
ClinVar
Risk rs864622280(C;C)
Alt rs864622280(C;C)
Reference rs864622280(G;G)
Significance Pathogenic
Disease Tumor susceptibility linked to germline BAP1 mutations Familial cancer of breast
Variation info
Gene PALB2
CLNDBN Tumor susceptibility linked to germline BAP1 mutations Familial cancer of breast
Reversed 1
HGVS NC_000016.9:g.23647326C>A; NC_000016.9:g.23647326C>G
CLNSRC
CLNACC RCV000219378.1, RCV000205547.1,