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

rs397507616

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs397507616(-;-)
Make rs397507616(-;A)
ReferenceGRCh38 38.1/141
Chromosome13
Position32336288
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507616
ebirs397507616
HLIrs397507616
Exacrs397507616
Varsomers397507616
Maprs397507616
PheGenIrs397507616
hapmaprs397507616
1000 genomesrs397507616
hgdprs397507616
ensemblrs397507616
gopubmedrs397507616
geneviewrs397507616
scholarrs397507616
googlers397507616
pharmgkbrs397507616
gwascentralrs397507616
openSNPrs397507616
23andMers397507616
23andMe allrs397507616
SNP Nexus

SNPshotrs397507616
SNPdbers397507616
MSV3drs397507616
GWAS Ctlgrs397507616
Max Magnitude0
ClinVar
Risk rs397507616(;)
Alt rs397507616(;)
Reference rs397507616(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.32910425delA
CLNSRC ClinVar
CLNACC RCV000043927.2,