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rs397507717

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397507717(C;T)
Make rs397507717(T;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position32326114
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507717
ebirs397507717
HLIrs397507717
Exacrs397507717
Varsomers397507717
Maprs397507717
PheGenIrs397507717
hapmaprs397507717
1000 genomesrs397507717
hgdprs397507717
ensemblrs397507717
gopubmedrs397507717
geneviewrs397507717
scholarrs397507717
googlers397507717
pharmgkbrs397507717
gwascentralrs397507717
openSNPrs397507717
23andMers397507717
23andMe allrs397507717
SNP Nexus

SNPshotrs397507717
SNPdbers397507717
MSV3drs397507717
GWAS Ctlgrs397507717
Max Magnitude0
ClinVar
Risk rs397507717(T;T)
Alt rs397507717(T;T)
Reference rs397507717(C;C)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast
Reversed 0
HGVS NC_000013.10:g.32900251C>T
CLNSRC ClinVar
CLNACC RCV000044405.2,