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rs876660193

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs876660193(-;-)
Make rs876660193(-;C)
ReferenceGRCh38.p2 38.2/147
Chromosome16
Position23629998
GenePALB2
is asnp
is mentioned by
dbSNPrs876660193
ebirs876660193
HLIrs876660193
Exacrs876660193
Varsomers876660193
Maprs876660193
PheGenIrs876660193
hapmaprs876660193
1000 genomesrs876660193
hgdprs876660193
ensemblrs876660193
gopubmedrs876660193
geneviewrs876660193
scholarrs876660193
googlers876660193
pharmgkbrs876660193
gwascentralrs876660193
openSNPrs876660193
23andMers876660193
23andMe allrs876660193
SNP Nexus

SNPshotrs876660193
SNPdbers876660193
MSV3drs876660193
GWAS Ctlgrs876660193
Max Magnitude0
ClinVar
Risk rs876660193(;)
Alt rs876660193(;)
Reference rs876660193(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.23641319delG
CLNSRC
CLNACC RCV000216333.1,