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rs397508937

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs397508937(-;-)
Make rs397508937(-;A)
ReferenceGRCh38 38.1/141
Chromosome17
Position43093445
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397508937
ebirs397508937
HLIrs397508937
Exacrs397508937
Varsomers397508937
Maprs397508937
PheGenIrs397508937
hapmaprs397508937
1000 genomesrs397508937
hgdprs397508937
ensemblrs397508937
gopubmedrs397508937
geneviewrs397508937
scholarrs397508937
googlers397508937
pharmgkbrs397508937
gwascentralrs397508937
openSNPrs397508937
23andMers397508937
23andMe allrs397508937
SNP Nexus

SNPshotrs397508937
SNPdbers397508937
MSV3drs397508937
GWAS Ctlgrs397508937
Max Magnitude0
ClinVar
Risk rs397508937(;)
Alt rs397508937(;)
Reference rs397508937(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.41245462delT
CLNSRC ClinVar
CLNACC RCV000047708.2,