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rs397508844

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(TGTT;TGTT) 0 common in clinvar
Make rs397508844(-;-)
Make rs397508844(-;TGTT)
ReferenceGRCh38 38.1/141
Chromosome17
Position43094353
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397508844
ebirs397508844
HLIrs397508844
Exacrs397508844
Varsomers397508844
Maprs397508844
PheGenIrs397508844
hapmaprs397508844
1000 genomesrs397508844
hgdprs397508844
ensemblrs397508844
gopubmedrs397508844
geneviewrs397508844
scholarrs397508844
googlers397508844
pharmgkbrs397508844
gwascentralrs397508844
openSNPrs397508844
23andMers397508844
23andMe allrs397508844
SNP Nexus

SNPshotrs397508844
SNPdbers397508844
MSV3drs397508844
GWAS Ctlgrs397508844
Max Magnitude0
ClinVar
Risk rs397508844(;)
Alt rs397508844(;)
Reference rs397508844(TGTT;TGTT)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA1
CLNDBN Familial cancer of breast
Reversed 1
HGVS NC_000017.10:g.41246370_41246373delAACA
CLNSRC ClinVar
CLNACC RCV000047371.2,