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rs397507783

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(GC;GC) 0 common in clinvar
Make rs397507783(-;-)
Make rs397507783(-;GC)
ReferenceGRCh38 38.1/141
Chromosome13
Position32339744
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507783
ebirs397507783
HLIrs397507783
Exacrs397507783
Varsomers397507783
Maprs397507783
PheGenIrs397507783
hapmaprs397507783
1000 genomesrs397507783
hgdprs397507783
ensemblrs397507783
gopubmedrs397507783
geneviewrs397507783
scholarrs397507783
googlers397507783
pharmgkbrs397507783
gwascentralrs397507783
openSNPrs397507783
23andMers397507783
23andMe allrs397507783
SNP Nexus

SNPshotrs397507783
SNPdbers397507783
MSV3drs397507783
GWAS Ctlgrs397507783
Max Magnitude0
ClinVar
Risk rs397507783(;)
Alt rs397507783(;)
Reference rs397507783(GC;GC)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast
Reversed 0
HGVS NC_000013.10:g.32913881_32913882delGC
CLNSRC ClinVar
CLNACC RCV000044646.2,