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rs397507766

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs397507766(-;-)
Make rs397507766(-;C)
Make rs397507766(C;C)
ReferenceGRCh38 38.1/141
Chromosome13
Position32326282
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507766
ebirs397507766
HLIrs397507766
Exacrs397507766
Varsomers397507766
Maprs397507766
PheGenIrs397507766
hapmaprs397507766
1000 genomesrs397507766
hgdprs397507766
ensemblrs397507766
gopubmedrs397507766
geneviewrs397507766
scholarrs397507766
googlers397507766
pharmgkbrs397507766
gwascentralrs397507766
openSNPrs397507766
23andMers397507766
23andMe allrs397507766
SNP Nexus

SNPshotrs397507766
SNPdbers397507766
MSV3drs397507766
GWAS Ctlgrs397507766
Max Magnitude0
ClinVar
Risk rs397507766(C;C)
Alt rs397507766(C;C)
Reference rs397507766(;)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast
Reversed 0
HGVS NC_000013.10:g.32900419_32900420insC
CLNSRC ClinVar
CLNACC RCV000044584.2,