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rs397507655

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(AGATATTGAAGAACA;AGATATTGAAGAACA) 0 common in clinvar
Make rs397507655(AGATATTGAAGAACA;T)
Make rs397507655(T;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position32337451
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507655
ebirs397507655
HLIrs397507655
Exacrs397507655
Varsomers397507655
Maprs397507655
PheGenIrs397507655
hapmaprs397507655
1000 genomesrs397507655
hgdprs397507655
ensemblrs397507655
gopubmedrs397507655
geneviewrs397507655
scholarrs397507655
googlers397507655
pharmgkbrs397507655
gwascentralrs397507655
openSNPrs397507655
23andMers397507655
23andMe allrs397507655
SNP Nexus

SNPshotrs397507655
SNPdbers397507655
MSV3drs397507655
GWAS Ctlgrs397507655
Max Magnitude0
ClinVar
Risk rs397507655(T;T)
Alt rs397507655(T;T)
Reference rs397507655(AGATATTGAAGAACA;AGATATTGAAGAACA)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast
Reversed 0
HGVS NC_000013.10:g.32911588_32911602delAGATATTGAAGAACAinsT
CLNSRC ClinVar
CLNACC RCV000044118.2,