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rs1060501729

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1060501729(-;-)
Make rs1060501729(-;A)
ReferenceGRCh38.p7 38.3/150
Chromosome17
Position61784388
GeneBRIP1
is asnp
is mentioned by
dbSNPrs1060501729
dbSNP (old)rs1060501729
ClinGenrs1060501729
ebirs1060501729
HLIrs1060501729
Exacrs1060501729
Gnomadrs1060501729
Varsomers1060501729
Maprs1060501729
PheGenIrs1060501729
Biobankrs1060501729
1000 genomesrs1060501729
hgdprs1060501729
ensemblrs1060501729
gopubmedrs1060501729
geneviewrs1060501729
scholarrs1060501729
googlers1060501729
pharmgkbrs1060501729
gwascentralrs1060501729
openSNPrs1060501729
23andMers1060501729
23andMe allrs1060501729
SNPshotrs1060501729
SNPdbers1060501729
MSV3drs1060501729
GWAS Ctlgrs1060501729
Max Magnitude0
ClinVar
Risk rs1060501729(-;-)
Alt rs1060501729(-;-)
Reference Rs1060501729(A;A)
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.59861749delT
CLNSRC
CLNACC RCV000464669.1,