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rs397509208

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs397509208(-;-)
Make rs397509208(-;A)
ReferenceGRCh38 38.1/141
Chromosome17
Position43070969
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397509208
ebirs397509208
HLIrs397509208
Exacrs397509208
Varsomers397509208
Maprs397509208
PheGenIrs397509208
hapmaprs397509208
1000 genomesrs397509208
hgdprs397509208
ensemblrs397509208
gopubmedrs397509208
geneviewrs397509208
scholarrs397509208
googlers397509208
pharmgkbrs397509208
gwascentralrs397509208
openSNPrs397509208
23andMers397509208
23andMe allrs397509208
SNP Nexus

SNPshotrs397509208
SNPdbers397509208
MSV3drs397509208
GWAS Ctlgrs397509208
Max Magnitude0
ClinVar
Risk rs397509208(;)
Alt rs397509208(;)
Reference rs397509208(A;A)
Significance Pathogenic
Disease Familial cancer of breast Breast-ovarian cancer not specified
Variation info
Gene BRCA1
CLNDBN Familial cancer of breast Breast-ovarian cancer, familial 1 not specified
Reversed 1
HGVS NC_000017.10:g.41222986delT
CLNSRC Breast Cancer Information Core (BRCA1)
CLNACC RCV000048705.2, RCV000112431.1, RCV000239002.1,