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rs397507834

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs397507834(-;-)
Make rs397507834(-;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position32340561
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507834
ebirs397507834
HLIrs397507834
Exacrs397507834
Varsomers397507834
Maprs397507834
PheGenIrs397507834
hapmaprs397507834
1000 genomesrs397507834
hgdprs397507834
ensemblrs397507834
gopubmedrs397507834
geneviewrs397507834
scholarrs397507834
googlers397507834
pharmgkbrs397507834
gwascentralrs397507834
openSNPrs397507834
23andMers397507834
23andMe allrs397507834
SNP Nexus

SNPshotrs397507834
SNPdbers397507834
MSV3drs397507834
GWAS Ctlgrs397507834
Max Magnitude0
ClinVar
Risk rs397507834(;)
Alt rs397507834(;)
Reference rs397507834(T;T)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast
Reversed 0
HGVS NC_000013.10:g.32914698delT
CLNSRC ClinVar
CLNACC RCV000044868.2,