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rs587781321

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587781321(A;A)
Make rs587781321(A;C)
ReferenceGRCh38.p2 38.2/144
Chromosome17
Position61780325
GeneBRIP1
is asnp
is mentioned by
dbSNPrs587781321
ebirs587781321
HLIrs587781321
Exacrs587781321
Varsomers587781321
Maprs587781321
PheGenIrs587781321
hapmaprs587781321
1000 genomesrs587781321
hgdprs587781321
ensemblrs587781321
gopubmedrs587781321
geneviewrs587781321
scholarrs587781321
googlers587781321
pharmgkbrs587781321
gwascentralrs587781321
openSNPrs587781321
23andMers587781321
23andMe allrs587781321
SNP Nexus

SNPshotrs587781321
SNPdbers587781321
MSV3drs587781321
GWAS Ctlgrs587781321
Max Magnitude0
ClinVar
Risk rs587781321(A,T;A,T)
Alt rs587781321(A,T;A,T)
Reference rs587781321(C;C)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome Familial cancer of breast Fanconi anemia
Variation info
Gene BRIP1
CLNDBN Hereditary cancer-predisposing syndrome Familial cancer of breast Fanconi anemia, complementation group J
Reversed 1
HGVS NC_000017.10:g.59857686G>A; NC_000017.10:g.59857686G>T
CLNSRC
CLNACC RCV000166032.1, RCV000197937.1, RCV000129060.3, RCV000228701.1,