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

rs397507594

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397507594(-;-)
Make rs397507594(-;G)
ReferenceGRCh38 38.1/141
Chromosome13
Position32333050
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507594
ebirs397507594
HLIrs397507594
Exacrs397507594
Varsomers397507594
Maprs397507594
PheGenIrs397507594
hapmaprs397507594
1000 genomesrs397507594
hgdprs397507594
ensemblrs397507594
gopubmedrs397507594
geneviewrs397507594
scholarrs397507594
googlers397507594
pharmgkbrs397507594
gwascentralrs397507594
openSNPrs397507594
23andMers397507594
23andMe allrs397507594
SNP Nexus

SNPshotrs397507594
SNPdbers397507594
MSV3drs397507594
GWAS Ctlgrs397507594
Max Magnitude0
ClinVar
Risk rs397507594(;)
Alt rs397507594(;)
Reference rs397507594(G;G)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast
Reversed 0
HGVS NC_000013.10:g.32907187delG
CLNSRC ClinVar
CLNACC RCV000043831.2,