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rs397508954

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(CTCAT;CTCAT) 0 common in clinvar
Make rs397508954(-;-)
Make rs397508954(-;CTCAT)
ReferenceGRCh38 38.1/141
Chromosome17
Position43093279
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397508954
ebirs397508954
HLIrs397508954
Exacrs397508954
Varsomers397508954
Maprs397508954
PheGenIrs397508954
hapmaprs397508954
1000 genomesrs397508954
hgdprs397508954
ensemblrs397508954
gopubmedrs397508954
geneviewrs397508954
scholarrs397508954
googlers397508954
pharmgkbrs397508954
gwascentralrs397508954
openSNPrs397508954
23andMers397508954
23andMe allrs397508954
SNP Nexus

SNPshotrs397508954
SNPdbers397508954
MSV3drs397508954
GWAS Ctlgrs397508954
Max Magnitude0
ClinVar
Risk rs397508954(;)
Alt rs397508954(;)
Reference rs397508954(CTCAT;CTCAT)
Significance Pathogenic
Disease Familial cancer of breast Breast-ovarian cancer
Variation info
Gene BRCA1
CLNDBN Familial cancer of breast Breast-ovarian cancer, familial 1
Reversed 1
HGVS NC_000017.10:g.41245296_41245300delATGAG
CLNSRC ClinVar
CLNACC RCV000047773.2, RCV000210960.1,