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rs864622568

From SNPedia

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Geno Mag Summary
(T;T) 0 common in clinvar
Make rs864622568(G;G)
Make rs864622568(G;T)
ReferenceGRCh38.p2 38.2/146
Chromosome13
Position32379823
GeneBRCA2
is asnp
is mentioned by
dbSNPrs864622568
ebirs864622568
HLIrs864622568
Exacrs864622568
Varsomers864622568
Maprs864622568
PheGenIrs864622568
hapmaprs864622568
1000 genomesrs864622568
hgdprs864622568
ensemblrs864622568
gopubmedrs864622568
geneviewrs864622568
scholarrs864622568
googlers864622568
pharmgkbrs864622568
gwascentralrs864622568
openSNPrs864622568
23andMers864622568
23andMe allrs864622568
SNP Nexus

SNPshotrs864622568
SNPdbers864622568
MSV3drs864622568
GWAS Ctlgrs864622568
Max Magnitude0
ClinVar
Risk rs864622568(G;G)
Alt rs864622568(G;G)
Reference rs864622568(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.32953960T>G
CLNSRC
CLNACC RCV000205381.1,