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rs397507612

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs397507612(-;-)
Make rs397507612(-;A)
ReferenceGRCh38 38.1/141
Chromosome13
Position32333359
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507612
ebirs397507612
HLIrs397507612
Exacrs397507612
Varsomers397507612
Maprs397507612
PheGenIrs397507612
hapmaprs397507612
1000 genomesrs397507612
hgdprs397507612
ensemblrs397507612
gopubmedrs397507612
geneviewrs397507612
scholarrs397507612
googlers397507612
pharmgkbrs397507612
gwascentralrs397507612
openSNPrs397507612
23andMers397507612
23andMe allrs397507612
SNP Nexus

SNPshotrs397507612
SNPdbers397507612
MSV3drs397507612
GWAS Ctlgrs397507612
Max Magnitude0
ClinVar
Risk rs397507612(;)
Alt rs397507612(;)
Reference rs397507612(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.32907496delA
CLNSRC ClinVar
CLNACC RCV000043915.2,