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

rs397507624

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397507624(A;A)
Make rs397507624(A;C)
ReferenceGRCh38 38.1/141
Chromosome13
Position32336727
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507624
ebirs397507624
HLIrs397507624
Exacrs397507624
Varsomers397507624
Maprs397507624
PheGenIrs397507624
hapmaprs397507624
1000 genomesrs397507624
hgdprs397507624
ensemblrs397507624
gopubmedrs397507624
geneviewrs397507624
scholarrs397507624
googlers397507624
pharmgkbrs397507624
gwascentralrs397507624
openSNPrs397507624
23andMers397507624
23andMe allrs397507624
SNP Nexus

SNPshotrs397507624
SNPdbers397507624
MSV3drs397507624
GWAS Ctlgrs397507624
Max Magnitude0
ClinVar
Risk rs397507624(A;A)
Alt rs397507624(A;A)
Reference rs397507624(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.32910864C>A
CLNSRC ClinVar
CLNACC RCV000043980.2,