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rs397507978

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(AG;AG) 0 common in clinvar
Make rs397507978(-;-)
Make rs397507978(-;AG)
ReferenceGRCh38 38.1/141
Chromosome13
Position32363532
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507978
ebirs397507978
HLIrs397507978
Exacrs397507978
Varsomers397507978
Maprs397507978
PheGenIrs397507978
hapmaprs397507978
1000 genomesrs397507978
hgdprs397507978
ensemblrs397507978
gopubmedrs397507978
geneviewrs397507978
scholarrs397507978
googlers397507978
pharmgkbrs397507978
gwascentralrs397507978
openSNPrs397507978
23andMers397507978
23andMe allrs397507978
SNP Nexus

SNPshotrs397507978
SNPdbers397507978
MSV3drs397507978
GWAS Ctlgrs397507978
Max Magnitude0
ClinVar
Risk rs397507978(;)
Alt rs397507978(;)
Reference rs397507978(AG;AG)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast
Reversed 0
HGVS NC_000013.10:g.32937669_32937670delAG
CLNSRC ClinVar
CLNACC RCV000045476.2,