Have questions? Visit https://www.reddit.com/r/SNPedia

rs876658157

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs876658157(A;A)
Make rs876658157(A;C)
ReferenceGRCh38.p2 38.2/147
Chromosome16
Position23614040
GenePALB2
is asnp
is mentioned by
dbSNPrs876658157
ebirs876658157
HLIrs876658157
Exacrs876658157
Varsomers876658157
Maprs876658157
PheGenIrs876658157
hapmaprs876658157
1000 genomesrs876658157
hgdprs876658157
ensemblrs876658157
gopubmedrs876658157
geneviewrs876658157
scholarrs876658157
googlers876658157
pharmgkbrs876658157
gwascentralrs876658157
openSNPrs876658157
23andMers876658157
23andMe allrs876658157
SNP Nexus

SNPshotrs876658157
SNPdbers876658157
MSV3drs876658157
GWAS Ctlgrs876658157
Max Magnitude0
ClinVar
Risk rs876658157(A;A)
Alt rs876658157(A;A)
Reference rs876658157(C;C)
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.23625361G>T
CLNSRC
CLNACC RCV000222632.1,