Have questions? Visit https://www.reddit.com/r/SNPedia

rs397508995

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(GA;GA) 0 common in clinvar
Make rs397508995(-;-)
Make rs397508995(-;GA)
ReferenceGRCh38 38.1/141
Chromosome17
Position43092851
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397508995
ebirs397508995
HLIrs397508995
Exacrs397508995
Varsomers397508995
Maprs397508995
PheGenIrs397508995
hapmaprs397508995
1000 genomesrs397508995
hgdprs397508995
ensemblrs397508995
gopubmedrs397508995
geneviewrs397508995
scholarrs397508995
googlers397508995
pharmgkbrs397508995
gwascentralrs397508995
openSNPrs397508995
23andMers397508995
23andMe allrs397508995
SNP Nexus

SNPshotrs397508995
SNPdbers397508995
MSV3drs397508995
GWAS Ctlgrs397508995
Max Magnitude0
ClinVar
Risk rs397508995(;)
Alt rs397508995(;)
Reference rs397508995(GA;GA)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA1
CLNDBN Familial cancer of breast
Reversed 1
HGVS NC_000017.10:g.41244868_41244869delTC
CLNSRC ClinVar
CLNACC RCV000047924.2,