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rs786201727

From SNPedia

Merged intors80359548
Orientationplus
Stabilizedplus
Geno Mag Summary
(-;-) 0 common in clinvar
(-;T) 6 BRCA2 variant considered pathogenic for breast cancer
Make rs786201727(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome13
Position32340289
GeneBRCA2
is asnp
is mentioned by
dbSNPrs786201727
dbSNP (old)rs786201727
ClinGenrs786201727
ebirs786201727
HLIrs786201727
Exacrs786201727
Varsomers786201727
Maprs786201727
PheGenIrs786201727
Biobankrs786201727
1000 genomesrs786201727
hgdprs786201727
ensemblrs786201727
gopubmedrs786201727
geneviewrs786201727
scholarrs786201727
googlers786201727
pharmgkbrs786201727
gwascentralrs786201727
openSNPrs786201727
23andMers786201727
23andMe allrs786201727
SNP Nexus

SNPshotrs786201727
SNPdbers786201727
MSV3drs786201727
GWAS Ctlgrs786201727
StatusMerged into rs80359548
Max Magnitude6
ClinVar
Risk rs786201727(T;T)
Alt rs786201727(T;T)
Reference Rs786201727(;)
Significance Pathogenic
Disease Breast-ovarian cancer Hereditary cancer-predisposing syndrome
Variation info
Gene BRCA2
CLNDBN Breast-ovarian cancer, familial 2 Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000013.10:g.32914426dupT
CLNSRC Breast Cancer Information Core (BRCA2)
CLNACC RCV000113505.3, RCV000164167.1,