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

rs1060501763

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1060501763(G;G)
Make rs1060501763(G;T)
ReferenceGRCh38.p7 38.3/150
Chromosome17
Position61859794
GeneBRIP1
is asnp
is mentioned by
dbSNPrs1060501763
dbSNP (old)rs1060501763
ClinGenrs1060501763
ebirs1060501763
HLIrs1060501763
Exacrs1060501763
Gnomadrs1060501763
Varsomers1060501763
LitVarrs1060501763
Maprs1060501763
PheGenIrs1060501763
Biobankrs1060501763
1000 genomesrs1060501763
hgdprs1060501763
ensemblrs1060501763
gopubmedrs1060501763
geneviewrs1060501763
scholarrs1060501763
googlers1060501763
pharmgkbrs1060501763
gwascentralrs1060501763
openSNPrs1060501763
23andMers1060501763
23andMe allrs1060501763
SNPshotrs1060501763
SNPdbers1060501763
MSV3drs1060501763
GWAS Ctlgrs1060501763
Max Magnitude0
ClinVar
Risk rs1060501763(G;G)
Alt rs1060501763(G;G)
Reference Rs1060501763(T;T)
Significance Probable-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.59937155A>C
CLNSRC
CLNACC RCV000460534.1,