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rs397507835

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397507835(-;-)
Make rs397507835(-;G)
ReferenceGRCh38 38.1/141
Chromosome13
Position32340590
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507835
ebirs397507835
HLIrs397507835
Exacrs397507835
Varsomers397507835
Maprs397507835
PheGenIrs397507835
hapmaprs397507835
1000 genomesrs397507835
hgdprs397507835
ensemblrs397507835
gopubmedrs397507835
geneviewrs397507835
scholarrs397507835
googlers397507835
pharmgkbrs397507835
gwascentralrs397507835
openSNPrs397507835
23andMers397507835
23andMe allrs397507835
SNP Nexus

SNPshotrs397507835
SNPdbers397507835
MSV3drs397507835
GWAS Ctlgrs397507835
Max Magnitude0
ClinVar
Risk rs397507835(;)
Alt rs397507835(;)
Reference rs397507835(G;G)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast
Reversed 0
HGVS NC_000013.10:g.32914727delG
CLNSRC ClinVar
CLNACC RCV000044876.2,