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rs1057517648

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057517648(-;-)
Make rs1057517648(-;G)
ReferenceGRCh38.p7 38.3/150
Chromosome17
Position61859795
GeneBRIP1
is asnp
is mentioned by
dbSNPrs1057517648
dbSNP (old)rs1057517648
ClinGenrs1057517648
ebirs1057517648
HLIrs1057517648
Exacrs1057517648
Gnomadrs1057517648
Varsomers1057517648
Maprs1057517648
PheGenIrs1057517648
Biobankrs1057517648
1000 genomesrs1057517648
hgdprs1057517648
ensemblrs1057517648
gopubmedrs1057517648
geneviewrs1057517648
scholarrs1057517648
googlers1057517648
pharmgkbrs1057517648
gwascentralrs1057517648
openSNPrs1057517648
23andMers1057517648
23andMe allrs1057517648
SNPshotrs1057517648
SNPdbers1057517648
MSV3drs1057517648
GWAS Ctlgrs1057517648
Max Magnitude0
ClinVar
Risk rs1057517648(-;-)
Alt rs1057517648(-;-)
Reference Rs1057517648(G;G)
Significance Probable-Pathogenic
Disease Neoplasm of ovary Fanconi anemia
Variation info
Gene BRIP1
CLNDBN Neoplasm of ovary Fanconi anemia, complementation group J
Reversed 1
HGVS NC_000017.10:g.59937156delC
CLNSRC
CLNACC RCV000410041.1, RCV000412391.1,