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rs397508982

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs397508982(-;-)
Make rs397508982(-;TTGAT)
Make rs397508982(TTGAT;TTGAT)
ReferenceGRCh38 38.1/141
Chromosome17
Position43092966
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397508982
ebirs397508982
HLIrs397508982
Exacrs397508982
Varsomers397508982
Maprs397508982
PheGenIrs397508982
hapmaprs397508982
1000 genomesrs397508982
hgdprs397508982
ensemblrs397508982
gopubmedrs397508982
geneviewrs397508982
scholarrs397508982
googlers397508982
pharmgkbrs397508982
gwascentralrs397508982
openSNPrs397508982
23andMers397508982
23andMe allrs397508982
SNP Nexus

SNPshotrs397508982
SNPdbers397508982
MSV3drs397508982
GWAS Ctlgrs397508982
Max Magnitude0
ClinVar
Risk rs397508982(TTGAT;TTGAT)
Alt rs397508982(TTGAT;TTGAT)
Reference rs397508982(;)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA1
CLNDBN Familial cancer of breast
Reversed 1
HGVS NC_000017.10:g.41244983_41244984insATCAA
CLNSRC ClinVar
CLNACC RCV000047881.2,