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rs397507839

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs397507839(-;-)
Make rs397507839(-;A)
ReferenceGRCh38 38.1/141
Chromosome13
Position32340657
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507839
ebirs397507839
HLIrs397507839
Exacrs397507839
Varsomers397507839
Maprs397507839
PheGenIrs397507839
hapmaprs397507839
1000 genomesrs397507839
hgdprs397507839
ensemblrs397507839
gopubmedrs397507839
geneviewrs397507839
scholarrs397507839
googlers397507839
pharmgkbrs397507839
gwascentralrs397507839
openSNPrs397507839
23andMers397507839
23andMe allrs397507839
SNP Nexus

SNPshotrs397507839
SNPdbers397507839
MSV3drs397507839
GWAS Ctlgrs397507839
Max Magnitude0
ClinVar
Risk rs397507839(;)
Alt rs397507839(;)
Reference rs397507839(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.32914794delA
CLNSRC ClinVar
CLNACC RCV000044892.2,