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rs397507703

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs397507703(-;-)
Make rs397507703(-;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position32338450
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507703
ebirs397507703
HLIrs397507703
Exacrs397507703
Varsomers397507703
Maprs397507703
PheGenIrs397507703
hapmaprs397507703
1000 genomesrs397507703
hgdprs397507703
ensemblrs397507703
gopubmedrs397507703
geneviewrs397507703
scholarrs397507703
googlers397507703
pharmgkbrs397507703
gwascentralrs397507703
openSNPrs397507703
23andMers397507703
23andMe allrs397507703
SNP Nexus

SNPshotrs397507703
SNPdbers397507703
MSV3drs397507703
GWAS Ctlgrs397507703
Max Magnitude0
ClinVar
Risk rs397507703(;)
Alt rs397507703(;)
Reference rs397507703(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.32912587delT
CLNSRC ClinVar
CLNACC RCV000044348.2,