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rs397508965

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397508965(-;-)
Make rs397508965(-;G)
ReferenceGRCh38 38.1/141
Chromosome17
Position43093142
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397508965
ebirs397508965
HLIrs397508965
Exacrs397508965
Varsomers397508965
Maprs397508965
PheGenIrs397508965
hapmaprs397508965
1000 genomesrs397508965
hgdprs397508965
ensemblrs397508965
gopubmedrs397508965
geneviewrs397508965
scholarrs397508965
googlers397508965
pharmgkbrs397508965
gwascentralrs397508965
openSNPrs397508965
23andMers397508965
23andMe allrs397508965
SNP Nexus

SNPshotrs397508965
SNPdbers397508965
MSV3drs397508965
GWAS Ctlgrs397508965
Max Magnitude0
ClinVar
Risk rs397508965(;)
Alt rs397508965(;)
Reference rs397508965(G;G)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA1
CLNDBN Familial cancer of breast
Reversed 1
HGVS NC_000017.10:g.41245159delC
CLNSRC ClinVar
CLNACC RCV000047821.2,