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rs1060501778

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1060501778(-;-)
Make rs1060501778(-;T)
ReferenceGRCh38.p7 38.3/150
Chromosome17
Position61847180
GeneBRIP1
is asnp
is mentioned by
dbSNPrs1060501778
dbSNP (old)rs1060501778
ClinGenrs1060501778
ebirs1060501778
HLIrs1060501778
Exacrs1060501778
Gnomadrs1060501778
Varsomers1060501778
Maprs1060501778
PheGenIrs1060501778
Biobankrs1060501778
1000 genomesrs1060501778
hgdprs1060501778
ensemblrs1060501778
gopubmedrs1060501778
geneviewrs1060501778
scholarrs1060501778
googlers1060501778
pharmgkbrs1060501778
gwascentralrs1060501778
openSNPrs1060501778
23andMers1060501778
23andMe allrs1060501778
SNPshotrs1060501778
SNPdbers1060501778
MSV3drs1060501778
GWAS Ctlgrs1060501778
Max Magnitude0
ClinVar
Risk rs1060501778(-;-)
Alt rs1060501778(-;-)
Reference Rs1060501778(T;T)
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.59924541delA
CLNSRC
CLNACC RCV000475128.1,