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rs397508956

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs397508956(-;-)
Make rs397508956(-;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position43093223
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397508956
ebirs397508956
HLIrs397508956
Exacrs397508956
Varsomers397508956
Maprs397508956
PheGenIrs397508956
hapmaprs397508956
1000 genomesrs397508956
hgdprs397508956
ensemblrs397508956
gopubmedrs397508956
geneviewrs397508956
scholarrs397508956
googlers397508956
pharmgkbrs397508956
gwascentralrs397508956
openSNPrs397508956
23andMers397508956
23andMe allrs397508956
SNP Nexus

SNPshotrs397508956
SNPdbers397508956
MSV3drs397508956
GWAS Ctlgrs397508956
Max Magnitude0
ClinVar
Risk rs397508956(;)
Alt rs397508956(;)
Reference rs397508956(T;T)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA1
CLNDBN Familial cancer of breast
Reversed 1
HGVS NC_000017.10:g.41245240delA
CLNSRC ClinVar
CLNACC RCV000047790.2,