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rs397508957

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397508957(C;GTCAACTTGTT)
Make rs397508957(GTCAACTTGTT;GTCAACTTGTT)
ReferenceGRCh38 38.1/141
Chromosome17
Position43104939
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397508957
ebirs397508957
HLIrs397508957
Exacrs397508957
Varsomers397508957
Maprs397508957
PheGenIrs397508957
hapmaprs397508957
1000 genomesrs397508957
hgdprs397508957
ensemblrs397508957
gopubmedrs397508957
geneviewrs397508957
scholarrs397508957
googlers397508957
pharmgkbrs397508957
gwascentralrs397508957
openSNPrs397508957
23andMers397508957
23andMe allrs397508957
SNP Nexus

SNPshotrs397508957
SNPdbers397508957
MSV3drs397508957
GWAS Ctlgrs397508957
Max Magnitude0
ClinVar
Risk rs397508957(GTCAACTTGTT;GTCAACTTGTT)
Alt rs397508957(GTCAACTTGTT;GTCAACTTGTT)
Reference rs397508957(C;C)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA1
CLNDBN Familial cancer of breast
Reversed 1
HGVS NC_000017.10:g.41256956delGinsAACAAGTTGAC
CLNSRC ClinVar
CLNACC RCV000047794.2,