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rs397507708

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs397507708(-;-)
Make rs397507708(-;A)
Make rs397507708(A;A)
ReferenceGRCh38 38.1/141
Chromosome13
Position32338491
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507708
ebirs397507708
HLIrs397507708
Exacrs397507708
Varsomers397507708
Maprs397507708
PheGenIrs397507708
hapmaprs397507708
1000 genomesrs397507708
hgdprs397507708
ensemblrs397507708
gopubmedrs397507708
geneviewrs397507708
scholarrs397507708
googlers397507708
pharmgkbrs397507708
gwascentralrs397507708
openSNPrs397507708
23andMers397507708
23andMe allrs397507708
SNP Nexus

SNPshotrs397507708
SNPdbers397507708
MSV3drs397507708
GWAS Ctlgrs397507708
Max Magnitude0
ClinVar
Risk rs397507708(A;A)
Alt rs397507708(A;A)
Reference rs397507708(;)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast
Reversed 0
HGVS NC_000013.10:g.32912628dupA
CLNSRC ClinVar
CLNACC RCV000044357.2,