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rs730881635

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs730881635(A;T)
Make rs730881635(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome17
Position61799284
GeneBRIP1
is asnp
is mentioned by
dbSNPrs730881635
ebirs730881635
HLIrs730881635
Exacrs730881635
Varsomers730881635
Maprs730881635
PheGenIrs730881635
hapmaprs730881635
1000 genomesrs730881635
hgdprs730881635
ensemblrs730881635
gopubmedrs730881635
geneviewrs730881635
scholarrs730881635
googlers730881635
pharmgkbrs730881635
gwascentralrs730881635
openSNPrs730881635
23andMers730881635
23andMe allrs730881635
SNP Nexus

SNPshotrs730881635
SNPdbers730881635
MSV3drs730881635
GWAS Ctlgrs730881635
Max Magnitude0
ClinVar
Risk rs730881635(T;T)
Alt rs730881635(T;T)
Reference rs730881635(A;A)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene BRIP1
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000017.10:g.59876645T>A
CLNSRC
CLNACC RCV000160337.1,