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rs864622082

From SNPedia

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Geno Mag Summary
(T;T) 0 common in clinvar
Make rs864622082(G;G)
Make rs864622082(G;T)
ReferenceGRCh38.p2 38.2/146
Chromosome13
Position32340609
GeneBRCA2
is asnp
is mentioned by
dbSNPrs864622082
ebirs864622082
HLIrs864622082
Exacrs864622082
Varsomers864622082
Maprs864622082
PheGenIrs864622082
hapmaprs864622082
1000 genomesrs864622082
hgdprs864622082
ensemblrs864622082
gopubmedrs864622082
geneviewrs864622082
scholarrs864622082
googlers864622082
pharmgkbrs864622082
gwascentralrs864622082
openSNPrs864622082
23andMers864622082
23andMe allrs864622082
SNP Nexus

SNPshotrs864622082
SNPdbers864622082
MSV3drs864622082
GWAS Ctlgrs864622082
Max Magnitude0
ClinVar
Risk rs864622082(G;G)
Alt rs864622082(G;G)
Reference rs864622082(T;T)
Significance Pathogenic
Disease Hereditary breast and ovarian cancer syndrome
Variation info
Gene BRCA2
CLNDBN Hereditary breast and ovarian cancer syndrome
Reversed 0
HGVS NC_000013.10:g.32914746T>G
CLNSRC
CLNACC RCV000204636.1,