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rs397507682

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(TAG;TAG) 0 common in clinvar
Make rs397507682(AT;AT)
Make rs397507682(AT;TAG)
ReferenceGRCh38 38.1/141
Chromosome13
Position32338078
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507682
ebirs397507682
HLIrs397507682
Exacrs397507682
Varsomers397507682
Maprs397507682
PheGenIrs397507682
hapmaprs397507682
1000 genomesrs397507682
hgdprs397507682
ensemblrs397507682
gopubmedrs397507682
geneviewrs397507682
scholarrs397507682
googlers397507682
pharmgkbrs397507682
gwascentralrs397507682
openSNPrs397507682
23andMers397507682
23andMe allrs397507682
SNP Nexus

SNPshotrs397507682
SNPdbers397507682
MSV3drs397507682
GWAS Ctlgrs397507682
Max Magnitude0
ClinVar
Risk rs397507682(AT;AT)
Alt rs397507682(AT;AT)
Reference rs397507682(TAG;TAG)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast
Reversed 0
HGVS NC_000013.10:g.32912215_32912217delTAGinsAT
CLNSRC ClinVar
CLNACC RCV000044251.2,