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rs397507727

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397507727(G;T)
Make rs397507727(T;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position32338907
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507727
ebirs397507727
HLIrs397507727
Exacrs397507727
Varsomers397507727
Maprs397507727
PheGenIrs397507727
hapmaprs397507727
1000 genomesrs397507727
hgdprs397507727
ensemblrs397507727
gopubmedrs397507727
geneviewrs397507727
scholarrs397507727
googlers397507727
pharmgkbrs397507727
gwascentralrs397507727
openSNPrs397507727
23andMers397507727
23andMe allrs397507727
SNP Nexus

SNPshotrs397507727
SNPdbers397507727
MSV3drs397507727
GWAS Ctlgrs397507727
Max Magnitude0
ClinVar
Risk rs397507727(T;T)
Alt rs397507727(T;T)
Reference rs397507727(G;G)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast
Reversed 0
HGVS NC_000013.10:g.32913044G>T
CLNSRC ClinVar
CLNACC RCV000044438.2,