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rs730881649

From SNPedia

Orientationminus
Geno Mag Summary
(AA;AA) 0 common in clinvar
Make rs730881649(-;-)
Make rs730881649(-;AA)
ReferenceGRCh38.p2 38.2/144
Chromosome17
Position61744433
GeneBRIP1, LOC105371851
is asnp
is mentioned by
dbSNPrs730881649
ebirs730881649
HLIrs730881649
Exacrs730881649
Varsomers730881649
Maprs730881649
PheGenIrs730881649
hapmaprs730881649
1000 genomesrs730881649
hgdprs730881649
ensemblrs730881649
gopubmedrs730881649
geneviewrs730881649
scholarrs730881649
googlers730881649
pharmgkbrs730881649
gwascentralrs730881649
openSNPrs730881649
23andMers730881649
23andMe allrs730881649
SNP Nexus

SNPshotrs730881649
SNPdbers730881649
MSV3drs730881649
GWAS Ctlgrs730881649
Max Magnitude0
ClinVar
Risk rs730881649(;)
Alt rs730881649(;)
Reference rs730881649(AA;AA)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome Familial cancer of breast Fanconi anemia not provided
Variation info
Gene BRIP1
CLNDBN Hereditary cancer-predisposing syndrome Familial cancer of breast Fanconi anemia, complementation group J not provided
Reversed 1
HGVS NC_000017.10:g.59821794_59821795delTT
CLNSRC Inc.
CLNACC RCV000160364.4, RCV000167986.2, RCV000212320.1,