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

rs397507222

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397507222(-;-)
Make rs397507222(-;C)
ReferenceGRCh38 38.1/141
Chromosome17
Position43091679
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397507222
ebirs397507222
HLIrs397507222
Exacrs397507222
Varsomers397507222
Maprs397507222
PheGenIrs397507222
hapmaprs397507222
1000 genomesrs397507222
hgdprs397507222
ensemblrs397507222
gopubmedrs397507222
geneviewrs397507222
scholarrs397507222
googlers397507222
pharmgkbrs397507222
gwascentralrs397507222
openSNPrs397507222
23andMers397507222
23andMe allrs397507222
SNP Nexus

SNPshotrs397507222
SNPdbers397507222
MSV3drs397507222
GWAS Ctlgrs397507222
Max Magnitude0
ClinVar
Risk rs397507222(;)
Alt rs397507222(;)
Reference rs397507222(C;C)
Significance Pathogenic
Disease Breast-ovarian cancer
Variation info
Gene BRCA1
CLNDBN Breast-ovarian cancer, familial 1
Reversed 1
HGVS NC_000017.10:g.41243696delG
CLNSRC ClinVar
CLNACC RCV000031133.3,