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rs1060501779

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1060501779(-;-)
Make rs1060501779(-;C)
ReferenceGRCh38.p7 38.3/150
Chromosome17
Position61808753
GeneBRIP1
is asnp
is mentioned by
dbSNPrs1060501779
dbSNP (old)rs1060501779
ClinGenrs1060501779
ebirs1060501779
HLIrs1060501779
Exacrs1060501779
Gnomadrs1060501779
Varsomers1060501779
LitVarrs1060501779
Maprs1060501779
PheGenIrs1060501779
Biobankrs1060501779
1000 genomesrs1060501779
hgdprs1060501779
ensemblrs1060501779
gopubmedrs1060501779
geneviewrs1060501779
scholarrs1060501779
googlers1060501779
pharmgkbrs1060501779
gwascentralrs1060501779
openSNPrs1060501779
23andMers1060501779
23andMe allrs1060501779
SNPshotrs1060501779
SNPdbers1060501779
MSV3drs1060501779
GWAS Ctlgrs1060501779
Max Magnitude0
ClinVar
Risk rs1060501779(-;-)
Alt rs1060501779(-;-)
Reference Rs1060501779(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.59886114delG
CLNSRC
CLNACC RCV000463454.1,