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rs397508872

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(GAGCGTCCCCTCACAA;GAGCGTCCCCTCACAA) 0 common in clinvar
Make rs397508872(-;-)
Make rs397508872(-;GAGCGTCCCCTCACAA)
ReferenceGRCh38 38.1/141
Chromosome17
Position43094033
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397508872
ebirs397508872
HLIrs397508872
Exacrs397508872
Varsomers397508872
Maprs397508872
PheGenIrs397508872
hapmaprs397508872
1000 genomesrs397508872
hgdprs397508872
ensemblrs397508872
gopubmedrs397508872
geneviewrs397508872
scholarrs397508872
googlers397508872
pharmgkbrs397508872
gwascentralrs397508872
openSNPrs397508872
23andMers397508872
23andMe allrs397508872
SNP Nexus

SNPshotrs397508872
SNPdbers397508872
MSV3drs397508872
GWAS Ctlgrs397508872
Max Magnitude0
ClinVar
Risk rs397508872(;)
Alt rs397508872(;)
Reference rs397508872(GAGCGTCCCCTCACAA;GAGCGTCCCCTCACAA)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA1
CLNDBN Familial cancer of breast
Reversed 1
HGVS NC_000017.10:g.41246050_41246065del16
CLNSRC ClinVar
CLNACC RCV000047491.2,