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rs397508936

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(AT;AT) 0 common in clinvar
Make rs397508936(-;-)
Make rs397508936(-;AT)
ReferenceGRCh38 38.1/141
Chromosome17
Position43093455
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397508936
ebirs397508936
HLIrs397508936
Exacrs397508936
Varsomers397508936
Maprs397508936
PheGenIrs397508936
hapmaprs397508936
1000 genomesrs397508936
hgdprs397508936
ensemblrs397508936
gopubmedrs397508936
geneviewrs397508936
scholarrs397508936
googlers397508936
pharmgkbrs397508936
gwascentralrs397508936
openSNPrs397508936
23andMers397508936
23andMe allrs397508936
SNP Nexus

SNPshotrs397508936
SNPdbers397508936
MSV3drs397508936
GWAS Ctlgrs397508936
Max Magnitude0
ClinVar
Risk rs397508936(;)
Alt rs397508936(;)
Reference rs397508936(AT;AT)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA1
CLNDBN Familial cancer of breast
Reversed 1
HGVS NC_000017.10:g.41245472_41245473delAT
CLNSRC ClinVar
CLNACC RCV000047701.2,