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rs1060501740

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1060501740(A;A)
Make rs1060501740(A;C)
ReferenceGRCh38.p7 38.3/150
Chromosome17
Position61857167
GeneBRIP1
is asnp
is mentioned by
dbSNPrs1060501740
dbSNP (classic)rs1060501740
ClinGenrs1060501740
ebirs1060501740
HLIrs1060501740
Exacrs1060501740
Gnomadrs1060501740
Varsomers1060501740
LitVarrs1060501740
Maprs1060501740
PheGenIrs1060501740
Biobankrs1060501740
1000 genomesrs1060501740
hgdprs1060501740
ensemblrs1060501740
geneviewrs1060501740
scholarrs1060501740
googlers1060501740
pharmgkbrs1060501740
gwascentralrs1060501740
openSNPrs1060501740
23andMers1060501740
23andMe allrs1060501740
SNPshotrs1060501740
SNPdbers1060501740
MSV3drs1060501740
GWAS Ctlgrs1060501740
Max Magnitude0
ClinVar
Risk rs1060501740(A;A)
Alt rs1060501740(A;A)
Reference Rs1060501740(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.59934528G>T
CLNSRC
CLNACC RCV000460420.1,