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rs397507767

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs397507767(-;-)
Make rs397507767(-;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position32339526
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507767
ebirs397507767
HLIrs397507767
Exacrs397507767
Varsomers397507767
Maprs397507767
PheGenIrs397507767
hapmaprs397507767
1000 genomesrs397507767
hgdprs397507767
ensemblrs397507767
gopubmedrs397507767
geneviewrs397507767
scholarrs397507767
googlers397507767
pharmgkbrs397507767
gwascentralrs397507767
openSNPrs397507767
23andMers397507767
23andMe allrs397507767
SNP Nexus

SNPshotrs397507767
SNPdbers397507767
MSV3drs397507767
GWAS Ctlgrs397507767
Max Magnitude0
ClinVar
Risk rs397507767(;)
Alt rs397507767(;)
Reference rs397507767(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.32913663delT
CLNSRC ClinVar
CLNACC RCV000044592.2,