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

rs878854930

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs878854930(-;-)
Make rs878854930(-;A)
ReferenceGRCh38.p2 38.2/147
Chromosome17
Position43094383
GeneBRCA1
is asnp
is mentioned by
dbSNPrs878854930
ebirs878854930
HLIrs878854930
Exacrs878854930
Varsomers878854930
Maprs878854930
PheGenIrs878854930
hapmaprs878854930
1000 genomesrs878854930
hgdprs878854930
ensemblrs878854930
gopubmedrs878854930
geneviewrs878854930
scholarrs878854930
googlers878854930
pharmgkbrs878854930
gwascentralrs878854930
openSNPrs878854930
23andMers878854930
23andMe allrs878854930
SNP Nexus

SNPshotrs878854930
SNPdbers878854930
MSV3drs878854930
GWAS Ctlgrs878854930
Max Magnitude0
ClinVar
Risk rs878854930(;)
Alt rs878854930(;)
Reference rs878854930(A;A)
Significance Pathogenic
Disease Hereditary breast and ovarian cancer syndrome
Variation info
Gene BRCA1
CLNDBN Hereditary breast and ovarian cancer syndrome
Reversed 1
HGVS NC_000017.10:g.41246400delT
CLNSRC
CLNACC RCV000232501.1,