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rs1060501757

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1060501757(G;T)
Make rs1060501757(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome17
Position61781006
GeneBRIP1
is asnp
is mentioned by
dbSNPrs1060501757
dbSNP (old)rs1060501757
ClinGenrs1060501757
ebirs1060501757
HLIrs1060501757
Exacrs1060501757
Gnomadrs1060501757
Varsomers1060501757
Maprs1060501757
PheGenIrs1060501757
Biobankrs1060501757
1000 genomesrs1060501757
hgdprs1060501757
ensemblrs1060501757
gopubmedrs1060501757
geneviewrs1060501757
scholarrs1060501757
googlers1060501757
pharmgkbrs1060501757
gwascentralrs1060501757
openSNPrs1060501757
23andMers1060501757
23andMe allrs1060501757
SNPshotrs1060501757
SNPdbers1060501757
MSV3drs1060501757
GWAS Ctlgrs1060501757
Max Magnitude0
ClinVar
Risk rs1060501757(T;T)
Alt rs1060501757(T;T)
Reference Rs1060501757(G;G)
Significance Probable-Pathogenic
Disease Familial cancer of breast Fanconi anemia
Variation info
Gene BRIP1
CLNDBN Familial cancer of breast Fanconi anemia, complementation group J
Reversed 1
HGVS NC_000017.10:g.59858367C>A
CLNSRC
CLNACC RCV000468302.1,