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rs397507679

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(GT;GT) 0 common in clinvar
Make rs397507679(GT;TAAAAAG)
Make rs397507679(TAAAAAG;TAAAAAG)
ReferenceGRCh38 38.1/141
Chromosome13
Position32338000
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507679
ebirs397507679
HLIrs397507679
Exacrs397507679
Varsomers397507679
Maprs397507679
PheGenIrs397507679
hapmaprs397507679
1000 genomesrs397507679
hgdprs397507679
ensemblrs397507679
gopubmedrs397507679
geneviewrs397507679
scholarrs397507679
googlers397507679
pharmgkbrs397507679
gwascentralrs397507679
openSNPrs397507679
23andMers397507679
23andMe allrs397507679
SNP Nexus

SNPshotrs397507679
SNPdbers397507679
MSV3drs397507679
GWAS Ctlgrs397507679
Max Magnitude0
ClinVar
Risk rs397507679(TAAAAAG;TAAAAAG)
Alt rs397507679(TAAAAAG;TAAAAAG)
Reference rs397507679(GT;GT)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast
Reversed 0
HGVS NC_000013.10:g.32912137_32912138delGTinsTAAAAAG
CLNSRC ClinVar
CLNACC RCV000044235.2,