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rs397507998

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs397507998(G;G)
Make rs397507998(G;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position32371102
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507998
ebirs397507998
HLIrs397507998
Exacrs397507998
Varsomers397507998
Maprs397507998
PheGenIrs397507998
hapmaprs397507998
1000 genomesrs397507998
hgdprs397507998
ensemblrs397507998
gopubmedrs397507998
geneviewrs397507998
scholarrs397507998
googlers397507998
pharmgkbrs397507998
gwascentralrs397507998
openSNPrs397507998
23andMers397507998
23andMe allrs397507998
SNP Nexus

SNPshotrs397507998
SNPdbers397507998
MSV3drs397507998
GWAS Ctlgrs397507998
Max Magnitude0
ClinVar
Risk rs397507998(G;G)
Alt rs397507998(G;G)
Reference rs397507998(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.32945239T>G
CLNSRC ClinVar
CLNACC RCV000045579.2,