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rs397507970

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs397507970(-;-)
Make rs397507970(-;A)
Make rs397507970(A;A)
ReferenceGRCh38 38.1/141
Chromosome13
Position32363430
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507970
ebirs397507970
HLIrs397507970
Exacrs397507970
Varsomers397507970
Maprs397507970
PheGenIrs397507970
hapmaprs397507970
1000 genomesrs397507970
hgdprs397507970
ensemblrs397507970
gopubmedrs397507970
geneviewrs397507970
scholarrs397507970
googlers397507970
pharmgkbrs397507970
gwascentralrs397507970
openSNPrs397507970
23andMers397507970
23andMe allrs397507970
SNP Nexus

SNPshotrs397507970
SNPdbers397507970
MSV3drs397507970
GWAS Ctlgrs397507970
Max Magnitude0
ClinVar
Risk rs397507970(A;A)
Alt rs397507970(A;A)
Reference rs397507970(;)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast
Reversed 0
HGVS NC_000013.10:g.32937567_32937568insA
CLNSRC ClinVar
CLNACC RCV000045455.2,