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rs606231397

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs606231397(-;-)
Make rs606231397(-;T)
Make rs606231397(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome13
Position32333086
GeneBRCA2
is asnp
is mentioned by
dbSNPrs606231397
ebirs606231397
HLIrs606231397
Exacrs606231397
Varsomers606231397
Maprs606231397
PheGenIrs606231397
hapmaprs606231397
1000 genomesrs606231397
hgdprs606231397
ensemblrs606231397
gopubmedrs606231397
geneviewrs606231397
scholarrs606231397
googlers606231397
pharmgkbrs606231397
gwascentralrs606231397
openSNPrs606231397
23andMers606231397
23andMe allrs606231397
SNP Nexus

SNPshotrs606231397
SNPdbers606231397
MSV3drs606231397
GWAS Ctlgrs606231397
Max Magnitude0
ClinVar
Risk rs606231397(T;T)
Alt rs606231397(T;T)
Reference rs606231397(;)
Significance Pathogenic
Disease Breast-ovarian cancer
Variation info
Gene BRCA2
CLNDBN Breast-ovarian cancer, familial 2
Reversed 0
HGVS NC_000013.10:g.32907223dupT
CLNSRC Breast Cancer Information Core (BRCA2)
CLNACC RCV000112942.1,