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rs747148023

From SNPedia

Orientationplus
Geno Mag Summary
(AG;AG) 0 common in clinvar
Make rs747148023(-;-)
Make rs747148023(-;AG)
ReferenceGRCh38.p2 38.2/147
Chromosome16
Position23629742
GenePALB2
is asnp
is mentioned by
dbSNPrs747148023
ebirs747148023
HLIrs747148023
Exacrs747148023
Varsomers747148023
Maprs747148023
PheGenIrs747148023
hapmaprs747148023
1000 genomesrs747148023
hgdprs747148023
ensemblrs747148023
gopubmedrs747148023
geneviewrs747148023
scholarrs747148023
googlers747148023
pharmgkbrs747148023
gwascentralrs747148023
openSNPrs747148023
23andMers747148023
23andMe allrs747148023
SNP Nexus

SNPshotrs747148023
SNPdbers747148023
MSV3drs747148023
GWAS Ctlgrs747148023
Max Magnitude0
ClinVar
Risk rs747148023(;)
Alt rs747148023(;)
Reference rs747148023(AG;AG)
Significance Pathogenic
Disease Tumor susceptibility linked to germline BAP1 mutations Familial cancer of breast not provided
Variation info
Gene PALB2
CLNDBN Tumor susceptibility linked to germline BAP1 mutations Familial cancer of breast not provided
Reversed 0
HGVS NC_000016.9:g.23641063_23641064delAG
CLNSRC
CLNACC RCV000218515.1, RCV000229872.1, RCV000236720.1,