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rs397507636

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(TG;TG) 0 common in clinvar
Make rs397507636(-;-)
Make rs397507636(-;TG)
ReferenceGRCh38 38.1/141
Chromosome13
Position32336992
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507636
ebirs397507636
HLIrs397507636
Exacrs397507636
Varsomers397507636
Maprs397507636
PheGenIrs397507636
hapmaprs397507636
1000 genomesrs397507636
hgdprs397507636
ensemblrs397507636
gopubmedrs397507636
geneviewrs397507636
scholarrs397507636
googlers397507636
pharmgkbrs397507636
gwascentralrs397507636
openSNPrs397507636
23andMers397507636
23andMe allrs397507636
SNP Nexus

SNPshotrs397507636
SNPdbers397507636
MSV3drs397507636
GWAS Ctlgrs397507636
Max Magnitude0
ClinVar
Risk rs397507636(;)
Alt rs397507636(;)
Reference rs397507636(TG;TG)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast
Reversed 0
HGVS NC_000013.10:g.32911129_32911130delTG
CLNSRC ClinVar
CLNACC RCV000044030.2,