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rs397507813

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(TGGAA;TGGAA) 0 common in clinvar
Make rs397507813(-;-)
Make rs397507813(-;TGGAA)
ReferenceGRCh38 38.1/141
Chromosome13
Position32340301
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507813
ebirs397507813
HLIrs397507813
Exacrs397507813
Varsomers397507813
Maprs397507813
PheGenIrs397507813
hapmaprs397507813
1000 genomesrs397507813
hgdprs397507813
ensemblrs397507813
gopubmedrs397507813
geneviewrs397507813
scholarrs397507813
googlers397507813
pharmgkbrs397507813
gwascentralrs397507813
openSNPrs397507813
23andMers397507813
23andMe allrs397507813
SNP Nexus

SNPshotrs397507813
SNPdbers397507813
MSV3drs397507813
GWAS Ctlgrs397507813
Max Magnitude0
ClinVar
Risk rs397507813(;)
Alt rs397507813(;)
Reference rs397507813(TGGAA;TGGAA)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast
Reversed 0
HGVS NC_000013.10:g.32914438_32914442delTGGAA
CLNSRC ClinVar
CLNACC RCV000044799.2,