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rs786202600

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;-) 0 common in clinvar
(-;T) 6 BRCA2 variant considered pathogenic for breast cancer
Make rs786202600(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome13
Position32354950
GeneBRCA2
is asnp
is mentioned by
dbSNPrs786202600
dbSNP (old)rs786202600
ClinGenrs786202600
ebirs786202600
HLIrs786202600
Exacrs786202600
Varsomers786202600
Maprs786202600
PheGenIrs786202600
Biobankrs786202600
1000 genomesrs786202600
hgdprs786202600
ensemblrs786202600
gopubmedrs786202600
geneviewrs786202600
scholarrs786202600
googlers786202600
pharmgkbrs786202600
gwascentralrs786202600
openSNPrs786202600
23andMers786202600
23andMe allrs786202600
SNP Nexus

SNPshotrs786202600
SNPdbers786202600
MSV3drs786202600
GWAS Ctlgrs786202600
Max Magnitude6
ClinVar
Risk rs786202600(T;T)
Alt rs786202600(T;T)
Reference Rs786202600(-;-)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome Breast-ovarian cancer
Variation info
Gene BRCA2
CLNDBN Hereditary cancer-predisposing syndrome Breast-ovarian cancer, familial 2
Reversed 0
HGVS NC_000013.10:g.32929087dupT
CLNSRC
CLNACC RCV000165488.1, RCV000241189.2,