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rs878854938

From SNPedia

Orientationminus
Geno Mag Summary
(TA;TA) 0 common in clinvar
Make rs878854938(-;-)
Make rs878854938(-;TA)
ReferenceGRCh38.p2 38.2/147
Chromosome17
Position43093304
GeneBRCA1
is asnp
is mentioned by
dbSNPrs878854938
ebirs878854938
HLIrs878854938
Exacrs878854938
Varsomers878854938
Maprs878854938
PheGenIrs878854938
hapmaprs878854938
1000 genomesrs878854938
hgdprs878854938
ensemblrs878854938
gopubmedrs878854938
geneviewrs878854938
scholarrs878854938
googlers878854938
pharmgkbrs878854938
gwascentralrs878854938
openSNPrs878854938
23andMers878854938
23andMe allrs878854938
SNP Nexus

SNPshotrs878854938
SNPdbers878854938
MSV3drs878854938
GWAS Ctlgrs878854938
Max Magnitude0
ClinVar
Risk rs878854938(;)
Alt rs878854938(;)
Reference rs878854938(TA;TA)
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.41245321_41245322delTA
CLNSRC
CLNACC RCV000231631.1,