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rs1057517643

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1057517643(A;A)
Make rs1057517643(A;T)
ReferenceGRCh38.p7 38.3/150
Chromosome17
Position61744578
GeneBRIP1
is asnp
is mentioned by
dbSNPrs1057517643
dbSNP (old)rs1057517643
ClinGenrs1057517643
ebirs1057517643
HLIrs1057517643
Exacrs1057517643
Gnomadrs1057517643
Varsomers1057517643
LitVarrs1057517643
Maprs1057517643
PheGenIrs1057517643
Biobankrs1057517643
1000 genomesrs1057517643
hgdprs1057517643
ensemblrs1057517643
gopubmedrs1057517643
geneviewrs1057517643
scholarrs1057517643
googlers1057517643
pharmgkbrs1057517643
gwascentralrs1057517643
openSNPrs1057517643
23andMers1057517643
23andMe allrs1057517643
SNPshotrs1057517643
SNPdbers1057517643
MSV3drs1057517643
GWAS Ctlgrs1057517643
Max Magnitude0
ClinVar
Risk rs1057517643(A;A)
Alt rs1057517643(A;A)
Reference Rs1057517643(T;T)
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.59821939A>T
CLNSRC
CLNACC RCV000409317.1, RCV000411722.1,