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rs397509188

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(-;CC) 6 BRCA1 variant considered pathogenic for breast cancer
(CC;CC) 0 common in clinvar


Make rs397509188(-;-)
ReferenceGRCh38 38.1/141
Chromosome17
Position43071229
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397509188
dbSNP (old)rs397509188
ClinGenrs397509188
ebirs397509188
HLIrs397509188
Exacrs397509188
Gnomadrs397509188
Varsomers397509188
Maprs397509188
PheGenIrs397509188
Biobankrs397509188
1000 genomesrs397509188
hgdprs397509188
ensemblrs397509188
gopubmedrs397509188
geneviewrs397509188
scholarrs397509188
googlers397509188
pharmgkbrs397509188
gwascentralrs397509188
openSNPrs397509188
23andMers397509188
23andMe allrs397509188
SNP Nexus

SNPshotrs397509188
SNPdbers397509188
MSV3drs397509188
GWAS Ctlgrs397509188
Max Magnitude6
ClinVar
Risk rs397509188(-;-)
Alt rs397509188(-;-)
Reference Rs397509188(CC;CC)
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.41223246_41223247delGG
CLNSRC ClinVar
CLNACC RCV000048629.2, RCV000241086.2,