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

rs397508007

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397508007(C;C)
Make rs397508007(C;G)
ReferenceGRCh38 38.1/141
Chromosome13
Position32376794
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397508007
ebirs397508007
HLIrs397508007
Exacrs397508007
Varsomers397508007
Maprs397508007
PheGenIrs397508007
hapmaprs397508007
1000 genomesrs397508007
hgdprs397508007
ensemblrs397508007
gopubmedrs397508007
geneviewrs397508007
scholarrs397508007
googlers397508007
pharmgkbrs397508007
gwascentralrs397508007
openSNPrs397508007
23andMers397508007
23andMe allrs397508007
SNP Nexus

SNPshotrs397508007
SNPdbers397508007
MSV3drs397508007
GWAS Ctlgrs397508007
Max Magnitude0
ClinVar
Risk rs397508007(C;C)
Alt rs397508007(C;C)
Reference rs397508007(G;G)
Significance Probable-Pathogenic
Disease Hereditary breast and ovarian cancer syndrome Hereditary cancer-predisposing syndrome
Variation info
Gene BRCA2
CLNDBN Hereditary breast and ovarian cancer syndrome Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000013.10:g.32950931G>C
CLNSRC Ambry Genetics ClinVar
CLNACC RCV000045614.4, RCV000131319.2,