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rs606231398

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs606231398(-;-)
Make rs606231398(-;A)
Make rs606231398(A;A)
ReferenceGRCh38.p2 38.2/144
Chromosome13
Position32333285
GeneBRCA2
is asnp
is mentioned by
dbSNPrs606231398
ebirs606231398
HLIrs606231398
Exacrs606231398
Varsomers606231398
Maprs606231398
PheGenIrs606231398
hapmaprs606231398
1000 genomesrs606231398
hgdprs606231398
ensemblrs606231398
gopubmedrs606231398
geneviewrs606231398
scholarrs606231398
googlers606231398
pharmgkbrs606231398
gwascentralrs606231398
openSNPrs606231398
23andMers606231398
23andMe allrs606231398
SNP Nexus

SNPshotrs606231398
SNPdbers606231398
MSV3drs606231398
GWAS Ctlgrs606231398
Max Magnitude0
ClinVar
Risk rs606231398(A;A)
Alt rs606231398(A;A)
Reference rs606231398(;)
Significance Pathogenic
Disease Breast-ovarian cancer Hereditary breast and ovarian cancer syndrome Hereditary cancer-predisposing syndrome not provided
Variation info
Gene BRCA2
CLNDBN Breast-ovarian cancer, familial 2 Hereditary breast and ovarian cancer syndrome Hereditary cancer-predisposing syndrome not provided
Reversed 0
HGVS NC_000013.10:g.32907428dupA
CLNSRC Breast Cancer Information Core (BRCA2)
CLNACC RCV000031343.11, RCV000043897.6, RCV000131453.2, RCV000160269.2,