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rs397507635

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397507635(C;TTT)
Make rs397507635(TTT;TTT)
ReferenceGRCh38 38.1/141
Chromosome13
Position32336967
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507635
ebirs397507635
HLIrs397507635
Exacrs397507635
Varsomers397507635
Maprs397507635
PheGenIrs397507635
hapmaprs397507635
1000 genomesrs397507635
hgdprs397507635
ensemblrs397507635
gopubmedrs397507635
geneviewrs397507635
scholarrs397507635
googlers397507635
pharmgkbrs397507635
gwascentralrs397507635
openSNPrs397507635
23andMers397507635
23andMe allrs397507635
SNP Nexus

SNPshotrs397507635
SNPdbers397507635
MSV3drs397507635
GWAS Ctlgrs397507635
Max Magnitude0
ClinVar
Risk rs397507635(TTT;TTT)
Alt rs397507635(TTT;TTT)
Reference rs397507635(C;C)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast
Reversed 0
HGVS NC_000013.10:g.32911104delCinsTTT
CLNSRC ClinVar
CLNACC RCV000044027.2,