Have questions? Visit https://www.reddit.com/r/SNPedia

rs397508909

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
(C;G) 6 BRCA1 variant considered pathogenic for breast cancer
Make rs397508909(G;G)
ReferenceGRCh38 38.1/141
Chromosome17
Position43093723
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397508909
dbSNP (old)rs397508909
ClinGenrs397508909
ebirs397508909
HLIrs397508909
Exacrs397508909
Gnomadrs397508909
Varsomers397508909
Maprs397508909
PheGenIrs397508909
Biobankrs397508909
1000 genomesrs397508909
hgdprs397508909
ensemblrs397508909
gopubmedrs397508909
geneviewrs397508909
scholarrs397508909
googlers397508909
pharmgkbrs397508909
gwascentralrs397508909
openSNPrs397508909
23andMers397508909
23andMe allrs397508909
SNP Nexus

SNPshotrs397508909
SNPdbers397508909
MSV3drs397508909
GWAS Ctlgrs397508909
Max Magnitude6
ClinVar
Risk rs397508909(G;G)
Alt rs397508909(G;G)
Reference Rs397508909(C;C)
Significance Pathogenic
Disease Familial cancer of breast Breast-ovarian cancer
Variation info
Gene BRCA1
CLNDBN Familial cancer of breast Breast-ovarian cancer, familial 1
Reversed 1
HGVS NC_000017.10:g.41245740G>C
CLNSRC ClinVar
CLNACC RCV000047592.2, RCV000256524.2,