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rs397508901

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs397508901(-;-)
Make rs397508901(-;A)
Make rs397508901(A;A)
ReferenceGRCh38 38.1/141
Chromosome17
Position43093814
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397508901
ebirs397508901
HLIrs397508901
Exacrs397508901
Varsomers397508901
Maprs397508901
PheGenIrs397508901
hapmaprs397508901
1000 genomesrs397508901
hgdprs397508901
ensemblrs397508901
gopubmedrs397508901
geneviewrs397508901
scholarrs397508901
googlers397508901
pharmgkbrs397508901
gwascentralrs397508901
openSNPrs397508901
23andMers397508901
23andMe allrs397508901
SNP Nexus

SNPshotrs397508901
SNPdbers397508901
MSV3drs397508901
GWAS Ctlgrs397508901
Max Magnitude0
ClinVar
Risk rs397508901(A;A)
Alt rs397508901(A;A)
Reference rs397508901(;)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA1
CLNDBN Familial cancer of breast
Reversed 1
HGVS NC_000017.10:g.41245832dupT
CLNSRC ClinVar
CLNACC RCV000047568.2,