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rs397509011

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(GT;GT) 0 common in clinvar
Make rs397509011(-;-)
Make rs397509011(-;GT)
ReferenceGRCh38 38.1/141
Chromosome17
Position43092732
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397509011
ebirs397509011
HLIrs397509011
Exacrs397509011
Varsomers397509011
Maprs397509011
PheGenIrs397509011
hapmaprs397509011
1000 genomesrs397509011
hgdprs397509011
ensemblrs397509011
gopubmedrs397509011
geneviewrs397509011
scholarrs397509011
googlers397509011
pharmgkbrs397509011
gwascentralrs397509011
openSNPrs397509011
23andMers397509011
23andMe allrs397509011
SNP Nexus

SNPshotrs397509011
SNPdbers397509011
MSV3drs397509011
GWAS Ctlgrs397509011
Max Magnitude0
ClinVar
Risk rs397509011(;)
Alt rs397509011(;)
Reference rs397509011(GT;GT)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA1
CLNDBN Familial cancer of breast
Reversed 1
HGVS NC_000017.10:g.41244749_41244750delAC
CLNSRC ClinVar
CLNACC RCV000047972.2,