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rs397507807

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(CC;CC) 0 common in clinvar
Make rs397507807(-;-)
Make rs397507807(-;CC)
ReferenceGRCh38 38.1/141
Chromosome13
Position32340154
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507807
ebirs397507807
HLIrs397507807
Exacrs397507807
Varsomers397507807
Maprs397507807
PheGenIrs397507807
hapmaprs397507807
1000 genomesrs397507807
hgdprs397507807
ensemblrs397507807
gopubmedrs397507807
geneviewrs397507807
scholarrs397507807
googlers397507807
pharmgkbrs397507807
gwascentralrs397507807
openSNPrs397507807
23andMers397507807
23andMe allrs397507807
SNP Nexus

SNPshotrs397507807
SNPdbers397507807
MSV3drs397507807
GWAS Ctlgrs397507807
Max Magnitude0
ClinVar
Risk rs397507807(;)
Alt rs397507807(;)
Reference rs397507807(CC;CC)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast
Reversed 0
HGVS NC_000013.10:g.32914291_32914292delCC
CLNSRC ClinVar
CLNACC RCV000044760.2,