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rs864622200

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;T) 6 BRCA2 variant considered pathogenic for breast cancer
(T;T) 0 common in clinvar


Make rs864622200(A;A)
ReferenceGRCh38.p2 38.2/146
Chromosome13
Position32379783
GeneBRCA2
is asnp
is mentioned by
dbSNPrs864622200
dbSNP (old)rs864622200
ClinGenrs864622200
ebirs864622200
HLIrs864622200
Exacrs864622200
Gnomadrs864622200
Varsomers864622200
Maprs864622200
PheGenIrs864622200
Biobankrs864622200
1000 genomesrs864622200
hgdprs864622200
ensemblrs864622200
gopubmedrs864622200
geneviewrs864622200
scholarrs864622200
googlers864622200
pharmgkbrs864622200
gwascentralrs864622200
openSNPrs864622200
23andMers864622200
23andMe allrs864622200
SNP Nexus

SNPshotrs864622200
SNPdbers864622200
MSV3drs864622200
GWAS Ctlgrs864622200
Max Magnitude6
ClinVar
Risk rs864622200(A;A)
Alt rs864622200(A;A)
Reference Rs864622200(T;T)
Significance Pathogenic
Disease Hereditary breast and ovarian cancer syndrome Breast-ovarian cancer
Variation info
Gene BRCA2
CLNDBN Hereditary breast and ovarian cancer syndrome Breast-ovarian cancer, familial 2
Reversed 0
HGVS NC_000013.10:g.32953920T>A
CLNSRC
CLNACC RCV000204346.2, RCV000241094.1,