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rs397508064

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs397508064(-;-)
Make rs397508064(-;G)
Make rs397508064(G;G)
ReferenceGRCh38 38.1/141
Chromosome13
Position32398218
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397508064
ebirs397508064
HLIrs397508064
Exacrs397508064
Varsomers397508064
Maprs397508064
PheGenIrs397508064
hapmaprs397508064
1000 genomesrs397508064
hgdprs397508064
ensemblrs397508064
gopubmedrs397508064
geneviewrs397508064
scholarrs397508064
googlers397508064
pharmgkbrs397508064
gwascentralrs397508064
openSNPrs397508064
23andMers397508064
23andMe allrs397508064
SNP Nexus

SNPshotrs397508064
SNPdbers397508064
MSV3drs397508064
GWAS Ctlgrs397508064
Max Magnitude0
ClinVar
Risk rs397508064(G;G)
Alt rs397508064(G;G)
Reference rs397508064(;)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast
Reversed 0
HGVS NC_000013.10:g.32972355_32972356insG
CLNSRC ClinVar
CLNACC RCV000045888.2,