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rs397507567

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs397507567(-;-)
Make rs397507567(-;A)
ReferenceGRCh38 38.1/141
Chromosome13
Position32398584
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507567
ebirs397507567
HLIrs397507567
Exacrs397507567
Varsomers397507567
Maprs397507567
PheGenIrs397507567
hapmaprs397507567
1000 genomesrs397507567
hgdprs397507567
ensemblrs397507567
gopubmedrs397507567
geneviewrs397507567
scholarrs397507567
googlers397507567
pharmgkbrs397507567
gwascentralrs397507567
openSNPrs397507567
23andMers397507567
23andMe allrs397507567
SNP Nexus

SNPshotrs397507567
SNPdbers397507567
MSV3drs397507567
GWAS Ctlgrs397507567
Max Magnitude0
ClinVar
Risk rs397507567(;)
Alt rs397507567(;)
Reference rs397507567(A;A)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast
Reversed 0
HGVS NC_000013.10:g.32972721delA
CLNSRC ClinVar
CLNACC RCV000043707.2,