Have questions? Visit https://www.reddit.com/r/SNPedia

rs1060501739

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1060501739(C;T)
Make rs1060501739(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome17
Position61784403
GeneBRIP1
is asnp
is mentioned by
dbSNPrs1060501739
dbSNP (old)rs1060501739
ClinGenrs1060501739
ebirs1060501739
HLIrs1060501739
Exacrs1060501739
Gnomadrs1060501739
Varsomers1060501739
Maprs1060501739
PheGenIrs1060501739
Biobankrs1060501739
1000 genomesrs1060501739
hgdprs1060501739
ensemblrs1060501739
gopubmedrs1060501739
geneviewrs1060501739
scholarrs1060501739
googlers1060501739
pharmgkbrs1060501739
gwascentralrs1060501739
openSNPrs1060501739
23andMers1060501739
23andMe allrs1060501739
SNPshotrs1060501739
SNPdbers1060501739
MSV3drs1060501739
GWAS Ctlgrs1060501739
Max Magnitude0
ClinVar
Risk rs1060501739(T;T)
Alt rs1060501739(T;T)
Reference Rs1060501739(C;C)
Significance 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.59861764G>A
CLNSRC
CLNACC RCV000473198.1,