Have questions? Visit https://www.reddit.com/r/SNPedia

rs397508839

From SNPedia

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


Make rs397508839(-;-)
ReferenceGRCh38 38.1/141
Chromosome17
Position43094408
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397508839
dbSNP (classic)rs397508839
ClinGenrs397508839
ebirs397508839
HLIrs397508839
Exacrs397508839
Gnomadrs397508839
Varsomers397508839
LitVarrs397508839
Maprs397508839
PheGenIrs397508839
Biobankrs397508839
1000 genomesrs397508839
hgdprs397508839
ensemblrs397508839
geneviewrs397508839
scholarrs397508839
googlers397508839
pharmgkbrs397508839
gwascentralrs397508839
openSNPrs397508839
23andMers397508839
SNPshotrs397508839
SNPdbers397508839
MSV3drs397508839
GWAS Ctlgrs397508839
Max Magnitude6

aka c.787+335_787+336del

ClinVar
Risk rs397508839(-;-)
Alt rs397508839(-;-)
Reference Rs397508839(AC;AC)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA1
CLNDBN Familial cancer of breast
Reversed 1
HGVS NC_000017.10:g.41246425_41246426delGT
CLNSRC ClinVar
CLNACC RCV000047352.2,