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rs606231401

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs606231401(-;-)
Make rs606231401(-;T)
Make rs606231401(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome13
Position32338638
GeneBRCA2
is asnp
is mentioned by
dbSNPrs606231401
ebirs606231401
HLIrs606231401
Exacrs606231401
Varsomers606231401
Maprs606231401
PheGenIrs606231401
hapmaprs606231401
1000 genomesrs606231401
hgdprs606231401
ensemblrs606231401
gopubmedrs606231401
geneviewrs606231401
scholarrs606231401
googlers606231401
pharmgkbrs606231401
gwascentralrs606231401
openSNPrs606231401
23andMers606231401
23andMe allrs606231401
SNP Nexus

SNPshotrs606231401
SNPdbers606231401
MSV3drs606231401
GWAS Ctlgrs606231401
Max Magnitude0
ClinVar
Risk rs606231401(T;T)
Alt rs606231401(T;T)
Reference rs606231401(;)
Significance Other
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.32912776dupT
CLNSRC Breast Cancer Information Core (BRCA2) Inc.
CLNACC RCV000031473.8, RCV000044387.5, RCV000130074.3, RCV000160287.2,