Have questions? Visit https://www.reddit.com/r/SNPedia

rs397507614

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397507614(-;-)
Make rs397507614(-;C)
ReferenceGRCh38 38.1/141
Chromosome13
Position32333379
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507614
ebirs397507614
HLIrs397507614
Exacrs397507614
Varsomers397507614
Maprs397507614
PheGenIrs397507614
hapmaprs397507614
1000 genomesrs397507614
hgdprs397507614
ensemblrs397507614
gopubmedrs397507614
geneviewrs397507614
scholarrs397507614
googlers397507614
pharmgkbrs397507614
gwascentralrs397507614
openSNPrs397507614
23andMers397507614
23andMe allrs397507614
SNP Nexus

SNPshotrs397507614
SNPdbers397507614
MSV3drs397507614
GWAS Ctlgrs397507614
Max Magnitude0
ClinVar
Risk rs397507614(;)
Alt rs397507614(;)
Reference rs397507614(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.32907516delC
CLNSRC ClinVar
CLNACC RCV000043920.2,