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rs777421358

From SNPedia

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Geno Mag Summary
(C;C) 0 common in clinvar
Make rs777421358(C;T)
Make rs777421358(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome13
Position32337006
GeneBRCA2
is asnp
is mentioned by
dbSNPrs777421358
ebirs777421358
HLIrs777421358
Exacrs777421358
Varsomers777421358
Maprs777421358
PheGenIrs777421358
hapmaprs777421358
1000 genomesrs777421358
hgdprs777421358
ensemblrs777421358
gopubmedrs777421358
geneviewrs777421358
scholarrs777421358
googlers777421358
pharmgkbrs777421358
gwascentralrs777421358
openSNPrs777421358
23andMers777421358
23andMe allrs777421358
SNP Nexus

SNPshotrs777421358
SNPdbers777421358
MSV3drs777421358
GWAS Ctlgrs777421358
Max Magnitude0
ClinVar
Risk rs777421358(T;T)
Alt rs777421358(T;T)
Reference rs777421358(C;C)
Significance Pathogenic
Disease Tumor susceptibility linked to germline BAP1 mutations
Variation info
Gene BRCA2
CLNDBN Tumor susceptibility linked to germline BAP1 mutations
Reversed 0
HGVS NC_000013.10:g.32911143C>G
CLNSRC
CLNACC RCV000222044.1,