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rs730881548

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs730881548(G;T)
Make rs730881548(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome13
Position32341040
GeneBRCA2
is asnp
is mentioned by
dbSNPrs730881548
ebirs730881548
HLIrs730881548
Exacrs730881548
Varsomers730881548
Maprs730881548
PheGenIrs730881548
hapmaprs730881548
1000 genomesrs730881548
hgdprs730881548
ensemblrs730881548
gopubmedrs730881548
geneviewrs730881548
scholarrs730881548
googlers730881548
pharmgkbrs730881548
gwascentralrs730881548
openSNPrs730881548
23andMers730881548
23andMe allrs730881548
SNP Nexus

SNPshotrs730881548
SNPdbers730881548
MSV3drs730881548
GWAS Ctlgrs730881548
Max Magnitude0
ClinVar
Risk rs730881548(T;T)
Alt rs730881548(T;T)
Reference rs730881548(G;G)
Significance Pathogenic
Disease not provided Tumor susceptibility linked to germline BAP1 mutations
Variation info
Gene BRCA2
CLNDBN not provided Tumor susceptibility linked to germline BAP1 mutations
Reversed 0
HGVS NC_000013.10:g.32915177G>T
CLNSRC
CLNACC RCV000160118.2, RCV000216038.1,