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rs397507794

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(AAAATTTGCC;AAAATTTGCC) 0 common in clinvar
(ATTTGCCAAA;ATTTGCCAAA) 0 common in clinvar
Make rs397507794(-;-)
Make rs397507794(-;ATTTGCCAAA)
ReferenceGRCh38 38.1/141
Chromosome13
Position32340005
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507794
ebirs397507794
HLIrs397507794
Exacrs397507794
Varsomers397507794
Maprs397507794
PheGenIrs397507794
hapmaprs397507794
1000 genomesrs397507794
hgdprs397507794
ensemblrs397507794
gopubmedrs397507794
geneviewrs397507794
scholarrs397507794
googlers397507794
pharmgkbrs397507794
gwascentralrs397507794
openSNPrs397507794
23andMers397507794
23andMe allrs397507794
SNP Nexus

SNPshotrs397507794
SNPdbers397507794
MSV3drs397507794
GWAS Ctlgrs397507794
Max Magnitude0
ClinVar
Risk rs397507794(;)
Alt rs397507794(;)
Reference rs397507794(AAAATTTGCC;AAAATTTGCC)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast
Reversed 0
HGVS NC_000013.10:g.32914142_32914151delATTTGCCAAA
CLNSRC ClinVar
CLNACC RCV000044707.2,