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rs397508924

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs397508924(-;-)
Make rs397508924(-;G)
Make rs397508924(G;G)
ReferenceGRCh38 38.1/141
Chromosome17
Position43093567
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397508924
ebirs397508924
HLIrs397508924
Exacrs397508924
Varsomers397508924
Maprs397508924
PheGenIrs397508924
hapmaprs397508924
1000 genomesrs397508924
hgdprs397508924
ensemblrs397508924
gopubmedrs397508924
geneviewrs397508924
scholarrs397508924
googlers397508924
pharmgkbrs397508924
gwascentralrs397508924
openSNPrs397508924
23andMers397508924
23andMe allrs397508924
SNP Nexus

SNPshotrs397508924
SNPdbers397508924
MSV3drs397508924
GWAS Ctlgrs397508924
Max Magnitude0
ClinVar
Risk rs397508924(GA,TA;GA,TA)
Alt rs397508924(GA,TA;GA,TA)
Reference rs397508924(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.41245584_41245585insC; NC_000017.10:g.41245585dupA
CLNSRC ClinVar
CLNACC RCV000047663.2, RCV000047664.2,