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rs730881439

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs730881439(-;-)
Make rs730881439(-;A)
ReferenceGRCh38.p2 38.2/144
Chromosome17
Position43092593
GeneBRCA1
is asnp
is mentioned by
dbSNPrs730881439
ebirs730881439
HLIrs730881439
Exacrs730881439
Varsomers730881439
Maprs730881439
PheGenIrs730881439
hapmaprs730881439
1000 genomesrs730881439
hgdprs730881439
ensemblrs730881439
gopubmedrs730881439
geneviewrs730881439
scholarrs730881439
googlers730881439
pharmgkbrs730881439
gwascentralrs730881439
openSNPrs730881439
23andMers730881439
23andMe allrs730881439
SNP Nexus

SNPshotrs730881439
SNPdbers730881439
MSV3drs730881439
GWAS Ctlgrs730881439
Max Magnitude0
ClinVar
Risk rs730881439(;)
Alt rs730881439(;)
Reference rs730881439(A;A)
Significance Pathogenic
Disease Familial cancer of breast
Variation info
Gene BRCA1
CLNDBN Familial cancer of breast
Reversed 1
HGVS NC_000017.10:g.41244610delT
CLNSRC
CLNACC RCV000159843.1,