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rs397507738

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs397507738(-;-)
Make rs397507738(-;GACC)
Make rs397507738(GACC;GACC)
ReferenceGRCh38 38.1/141
Chromosome13
Position32339053
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507738
ebirs397507738
HLIrs397507738
Exacrs397507738
Varsomers397507738
Maprs397507738
PheGenIrs397507738
hapmaprs397507738
1000 genomesrs397507738
hgdprs397507738
ensemblrs397507738
gopubmedrs397507738
geneviewrs397507738
scholarrs397507738
googlers397507738
pharmgkbrs397507738
gwascentralrs397507738
openSNPrs397507738
23andMers397507738
23andMe allrs397507738
SNP Nexus

SNPshotrs397507738
SNPdbers397507738
MSV3drs397507738
GWAS Ctlgrs397507738
Max Magnitude0
ClinVar
Risk rs397507738(GACC;GACC)
Alt rs397507738(GACC;GACC)
Reference rs397507738(;)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast
Reversed 0
HGVS NC_000013.10:g.32913187_32913190dupGACC
CLNSRC ClinVar
CLNACC RCV000044471.2,