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rs1057519365

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(AA;AA) 0 common in clinvar
Make rs1057519365(-;-)
Make rs1057519365(-;AA)
ReferenceGRCh38.p7 38.3/150
Chromosome17
Position61780931
GeneBRIP1
is asnp
is mentioned by
dbSNPrs1057519365
dbSNP (classic)rs1057519365
ClinGenrs1057519365
ebirs1057519365
HLIrs1057519365
Exacrs1057519365
Gnomadrs1057519365
Varsomers1057519365
LitVarrs1057519365
Maprs1057519365
PheGenIrs1057519365
Biobankrs1057519365
1000 genomesrs1057519365
hgdprs1057519365
ensemblrs1057519365
geneviewrs1057519365
scholarrs1057519365
googlers1057519365
pharmgkbrs1057519365
gwascentralrs1057519365
openSNPrs1057519365
23andMers1057519365
23andMe allrs1057519365
SNPshotrs1057519365
SNPdbers1057519365
MSV3drs1057519365
GWAS Ctlgrs1057519365
Max Magnitude0
ClinVar
Risk rs1057519365(-;-)
Alt rs1057519365(-;-)
Reference Rs1057519365(AA;AA)
Significance Probable-Pathogenic
Disease Carcinoma of colon not provided
Variation info
Gene BRIP1
CLNDBN Carcinoma of colon not provided
Reversed 1
HGVS NC_000017.10:g.59858292_59858293delTT
CLNSRC
CLNACC RCV000416663.1, RCV000477976.1,