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rs201523522

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs201523522(C;T)
Make rs201523522(T;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position32319180
GeneBRCA2
is asnp
is mentioned by
dbSNPrs201523522
ebirs201523522
HLIrs201523522
Exacrs201523522
Varsomers201523522
Maprs201523522
PheGenIrs201523522
hapmaprs201523522
1000 genomesrs201523522
hgdprs201523522
ensemblrs201523522
gopubmedrs201523522
geneviewrs201523522
scholarrs201523522
googlers201523522
pharmgkbrs201523522
gwascentralrs201523522
openSNPrs201523522
23andMers201523522
23andMe allrs201523522
SNP Nexus

SNPshotrs201523522
SNPdbers201523522
MSV3drs201523522
GWAS Ctlgrs201523522
GMAF0.0004591
Max Magnitude0
ClinVar
Risk rs201523522(G,T;G,T)
Alt rs201523522(G,T;G,T)
Reference rs201523522(C;C)
Significance Pathogenic
Disease Tumor susceptibility linked to germline BAP1 mutations Familial cancer of breast
Variation info
Gene BRCA2
CLNDBN Tumor susceptibility linked to germline BAP1 mutations Familial cancer of breast
Reversed 0
HGVS NC_000013.10:g.32893317C>A; NC_000013.10:g.32893317C>G
CLNSRC ClinVar
CLNACC RCV000220700.1, RCV000043867.2,