Have questions? Visit https://www.reddit.com/r/SNPedia

rs397507600

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;TAATTGATAATGGA) 6 BRCA2 variant considered pathogenic for breast cancer
(TAATTGATAATGGA;TAATTGATAATGGA) 0 common in clinvar


Make rs397507600(-;-)
ReferenceGRCh38 38.1/141
Chromosome13
Position32333148
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507600
ClinGenrs397507600
ebirs397507600
HLIrs397507600
Exacrs397507600
Varsomers397507600
Maprs397507600
PheGenIrs397507600
hapmaprs397507600
1000 genomesrs397507600
hgdprs397507600
ensemblrs397507600
gopubmedrs397507600
geneviewrs397507600
scholarrs397507600
googlers397507600
pharmgkbrs397507600
gwascentralrs397507600
openSNPrs397507600
23andMers397507600
23andMe allrs397507600
SNP Nexus

SNPshotrs397507600
SNPdbers397507600
MSV3drs397507600
GWAS Ctlgrs397507600
Max Magnitude6
ClinVar
Risk rs397507600(-;-)
Alt rs397507600(-;-)
Reference Rs397507600(TAATTGATAATGGA;TAATTGATAATGGA)
Significance Pathogenic
Disease Familial cancer of breast Breast-ovarian cancer
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast Breast-ovarian cancer, familial 2
Reversed 0
HGVS NC_000013.10:g.32907285_32907298delTAATTGATAATGGA
CLNSRC ClinVar
CLNACC RCV000043858.2, RCV000257260.2,