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rs397508852

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(ACT;ACT) 0 common in clinvar
Make rs397508852(ACT;GA)
Make rs397508852(GA;GA)
ReferenceGRCh38 38.1/141
Chromosome17
Position43094236
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397508852
ebirs397508852
HLIrs397508852
Exacrs397508852
Varsomers397508852
Maprs397508852
PheGenIrs397508852
hapmaprs397508852
1000 genomesrs397508852
hgdprs397508852
ensemblrs397508852
gopubmedrs397508852
geneviewrs397508852
scholarrs397508852
googlers397508852
pharmgkbrs397508852
gwascentralrs397508852
openSNPrs397508852
23andMers397508852
23andMe allrs397508852
SNP Nexus

SNPshotrs397508852
SNPdbers397508852
MSV3drs397508852
GWAS Ctlgrs397508852
Max Magnitude0
ClinVar
Risk rs397508852(GA;GA)
Alt rs397508852(GA;GA)
Reference rs397508852(ACT;ACT)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA1
CLNDBN Familial cancer of breast
Reversed 1
HGVS NC_000017.10:g.41246253_41246255delAGTinsTC
CLNSRC ClinVar
CLNACC RCV000047407.2,