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rs397508846

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs397508846(-;-)
Make rs397508846(-;A)
ReferenceGRCh38 38.1/141
Chromosome17
Position43094314
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397508846
ebirs397508846
HLIrs397508846
Exacrs397508846
Varsomers397508846
Maprs397508846
PheGenIrs397508846
hapmaprs397508846
1000 genomesrs397508846
hgdprs397508846
ensemblrs397508846
gopubmedrs397508846
geneviewrs397508846
scholarrs397508846
googlers397508846
pharmgkbrs397508846
gwascentralrs397508846
openSNPrs397508846
23andMers397508846
23andMe allrs397508846
SNP Nexus

SNPshotrs397508846
SNPdbers397508846
MSV3drs397508846
GWAS Ctlgrs397508846
Max Magnitude0
ClinVar
Risk rs397508846(;)
Alt rs397508846(;)
Reference rs397508846(A;A)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA1
CLNDBN Familial cancer of breast
Reversed 1
HGVS NC_000017.10:g.41246331delT
CLNSRC ClinVar
CLNACC RCV000047381.2,