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rs397507648

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397507648(G;T)
Make rs397507648(T;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position32337305
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507648
ebirs397507648
HLIrs397507648
Exacrs397507648
Varsomers397507648
Maprs397507648
PheGenIrs397507648
hapmaprs397507648
1000 genomesrs397507648
hgdprs397507648
ensemblrs397507648
gopubmedrs397507648
geneviewrs397507648
scholarrs397507648
googlers397507648
pharmgkbrs397507648
gwascentralrs397507648
openSNPrs397507648
23andMers397507648
23andMe allrs397507648
SNP Nexus

SNPshotrs397507648
SNPdbers397507648
MSV3drs397507648
GWAS Ctlgrs397507648
Max Magnitude0
ClinVar
Risk rs397507648(T;T)
Alt rs397507648(T;T)
Reference rs397507648(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.32911442G>T
CLNSRC ClinVar
CLNACC RCV000044092.2,