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rs397507621

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs397507621(-;-)
Make rs397507621(-;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position32336614
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507621
ebirs397507621
HLIrs397507621
Exacrs397507621
Varsomers397507621
Maprs397507621
PheGenIrs397507621
hapmaprs397507621
1000 genomesrs397507621
hgdprs397507621
ensemblrs397507621
gopubmedrs397507621
geneviewrs397507621
scholarrs397507621
googlers397507621
pharmgkbrs397507621
gwascentralrs397507621
openSNPrs397507621
23andMers397507621
23andMe allrs397507621
SNP Nexus

SNPshotrs397507621
SNPdbers397507621
MSV3drs397507621
GWAS Ctlgrs397507621
Max Magnitude0
ClinVar
Risk rs397507621(;)
Alt rs397507621(;)
Reference rs397507621(T;T)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast
Reversed 0
HGVS NC_000013.10:g.32910751delT
CLNSRC ClinVar
CLNACC RCV000043963.2,