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rs760094988

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs760094988(G;T)
Make rs760094988(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome16
Position23630235
GenePALB2
is asnp
is mentioned by
dbSNPrs760094988
ebirs760094988
HLIrs760094988
Exacrs760094988
Varsomers760094988
Maprs760094988
PheGenIrs760094988
hapmaprs760094988
1000 genomesrs760094988
hgdprs760094988
ensemblrs760094988
gopubmedrs760094988
geneviewrs760094988
scholarrs760094988
googlers760094988
pharmgkbrs760094988
gwascentralrs760094988
openSNPrs760094988
23andMers760094988
23andMe allrs760094988
SNP Nexus

SNPshotrs760094988
SNPdbers760094988
MSV3drs760094988
GWAS Ctlgrs760094988
Max Magnitude0
ClinVar
Risk rs760094988(T;T)
Alt rs760094988(T;T)
Reference rs760094988(G;G)
Significance Pathogenic
Disease Tumor susceptibility linked to germline BAP1 mutations
Variation info
Gene PALB2
CLNDBN Tumor susceptibility linked to germline BAP1 mutations
Reversed 0
HGVS NC_000016.9:g.23641556G>T
CLNSRC
CLNACC RCV000214899.1,