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rs397507995

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs397507995(-;-)
Make rs397507995(-;T)
Make rs397507995(T;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position32371069
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507995
ebirs397507995
HLIrs397507995
Exacrs397507995
Varsomers397507995
Maprs397507995
PheGenIrs397507995
hapmaprs397507995
1000 genomesrs397507995
hgdprs397507995
ensemblrs397507995
gopubmedrs397507995
geneviewrs397507995
scholarrs397507995
googlers397507995
pharmgkbrs397507995
gwascentralrs397507995
openSNPrs397507995
23andMers397507995
23andMe allrs397507995
SNP Nexus

SNPshotrs397507995
SNPdbers397507995
MSV3drs397507995
GWAS Ctlgrs397507995
Max Magnitude0
ClinVar
Risk rs397507995(T;T)
Alt rs397507995(T;T)
Reference rs397507995(;)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast
Reversed 0
HGVS NC_000013.10:g.32945206dupT
CLNSRC ClinVar
CLNACC RCV000045572.2,