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rs876660465

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs876660465(A;A)
Make rs876660465(A;T)
ReferenceGRCh38.p2 38.2/147
Chromosome16
Position23636199
GenePALB2
is asnp
is mentioned by
dbSNPrs876660465
ebirs876660465
HLIrs876660465
Exacrs876660465
Varsomers876660465
Maprs876660465
PheGenIrs876660465
hapmaprs876660465
1000 genomesrs876660465
hgdprs876660465
ensemblrs876660465
gopubmedrs876660465
geneviewrs876660465
scholarrs876660465
googlers876660465
pharmgkbrs876660465
gwascentralrs876660465
openSNPrs876660465
23andMers876660465
23andMe allrs876660465
SNP Nexus

SNPshotrs876660465
SNPdbers876660465
MSV3drs876660465
GWAS Ctlgrs876660465
Max Magnitude0
ClinVar
Risk rs876660465(A;A)
Alt rs876660465(A;A)
Reference rs876660465(T;T)
Significance Pathogenic
Disease Tumor susceptibility linked to germline BAP1 mutations
Variation info
Gene PALB2
CLNDBN Tumor susceptibility linked to germline BAP1 mutations
Reversed 1
HGVS NC_000016.9:g.23647520A>T
CLNSRC
CLNACC RCV000223009.1,