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rs397507735

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(GAGAT;GAGAT) 0 common in clinvar
Make rs397507735(-;-)
Make rs397507735(-;GAGAT)
ReferenceGRCh38 38.1/141
Chromosome13
Position32326139
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507735
ebirs397507735
HLIrs397507735
Exacrs397507735
Varsomers397507735
Maprs397507735
PheGenIrs397507735
hapmaprs397507735
1000 genomesrs397507735
hgdprs397507735
ensemblrs397507735
gopubmedrs397507735
geneviewrs397507735
scholarrs397507735
googlers397507735
pharmgkbrs397507735
gwascentralrs397507735
openSNPrs397507735
23andMers397507735
23andMe allrs397507735
SNP Nexus

SNPshotrs397507735
SNPdbers397507735
MSV3drs397507735
GWAS Ctlgrs397507735
Max Magnitude0
ClinVar
Risk rs397507735(;)
Alt rs397507735(;)
Reference rs397507735(GAGAT;GAGAT)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast
Reversed 0
HGVS NC_000013.10:g.32900276_32900280delGAGAT
CLNSRC ClinVar
CLNACC RCV000044461.2,