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rs397507985

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs397507985(-;-)
Make rs397507985(-;A)
Make rs397507985(A;A)
ReferenceGRCh38 38.1/141
Chromosome13
Position32370485
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507985
ebirs397507985
HLIrs397507985
Exacrs397507985
Varsomers397507985
Maprs397507985
PheGenIrs397507985
hapmaprs397507985
1000 genomesrs397507985
hgdprs397507985
ensemblrs397507985
gopubmedrs397507985
geneviewrs397507985
scholarrs397507985
googlers397507985
pharmgkbrs397507985
gwascentralrs397507985
openSNPrs397507985
23andMers397507985
23andMe allrs397507985
SNP Nexus

SNPshotrs397507985
SNPdbers397507985
MSV3drs397507985
GWAS Ctlgrs397507985
Max Magnitude0
ClinVar
Risk rs397507985(A;A)
Alt rs397507985(A;A)
Reference rs397507985(;)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast
Reversed 0
HGVS NC_000013.10:g.32944622dupA
CLNSRC ClinVar
CLNACC RCV000045511.2,