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rs397507802

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs397507802(-;-)
Make rs397507802(-;A)
Make rs397507802(A;A)
ReferenceGRCh38 38.1/141
Chromosome13
Position32326556
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507802
ebirs397507802
HLIrs397507802
Exacrs397507802
Varsomers397507802
Maprs397507802
PheGenIrs397507802
hapmaprs397507802
1000 genomesrs397507802
hgdprs397507802
ensemblrs397507802
gopubmedrs397507802
geneviewrs397507802
scholarrs397507802
googlers397507802
pharmgkbrs397507802
gwascentralrs397507802
openSNPrs397507802
23andMers397507802
23andMe allrs397507802
SNP Nexus

SNPshotrs397507802
SNPdbers397507802
MSV3drs397507802
GWAS Ctlgrs397507802
Max Magnitude0
ClinVar
Risk rs397507802(A;A)
Alt rs397507802(A;A)
Reference rs397507802(;)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast
Reversed 0
HGVS NC_000013.10:g.32900693dupA
CLNSRC ClinVar
CLNACC RCV000044742.2,