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rs606231397

From SNPedia

Merged intors276174811
Orientationplus
Stabilizedplus
Geno Mag Summary
(-;-) 0 common in clinvar
(-;T) 6 BRCA2 variant considered pathogenic for breast cancer
Make rs606231397(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome13
Position32333086
GeneBRCA2
is asnp
is mentioned by
dbSNPrs606231397
dbSNP (old)rs606231397
ClinGenrs606231397
ebirs606231397
HLIrs606231397
Exacrs606231397
Gnomadrs606231397
Varsomers606231397
Maprs606231397
PheGenIrs606231397
Biobankrs606231397
1000 genomesrs606231397
hgdprs606231397
ensemblrs606231397
gopubmedrs606231397
geneviewrs606231397
scholarrs606231397
googlers606231397
pharmgkbrs606231397
gwascentralrs606231397
openSNPrs606231397
23andMers606231397
23andMe allrs606231397
SNP Nexus

SNPshotrs606231397
SNPdbers606231397
MSV3drs606231397
GWAS Ctlgrs606231397
StatusMerged into rs276174811
Max Magnitude6

rs606231397 has merged into rs276174811

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 RCV000112942.2,