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rs397508907

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(CA;CA) 0 common in clinvar
Make rs397508907(-;-)
Make rs397508907(-;CA)
ReferenceGRCh38 38.1/141
Chromosome17
Position43106489
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397508907
ebirs397508907
HLIrs397508907
Exacrs397508907
Varsomers397508907
Maprs397508907
PheGenIrs397508907
hapmaprs397508907
1000 genomesrs397508907
hgdprs397508907
ensemblrs397508907
gopubmedrs397508907
geneviewrs397508907
scholarrs397508907
googlers397508907
pharmgkbrs397508907
gwascentralrs397508907
openSNPrs397508907
23andMers397508907
23andMe allrs397508907
SNP Nexus

SNPshotrs397508907
SNPdbers397508907
MSV3drs397508907
GWAS Ctlgrs397508907
Max Magnitude0
ClinVar
Risk rs397508907(;)
Alt rs397508907(;)
Reference rs397508907(CA;CA)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA1
CLNDBN Familial cancer of breast
Reversed 1
HGVS NC_000017.10:g.41258506_41258507delTG
CLNSRC ClinVar
CLNACC RCV000047586.2,