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rs1057520058

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(AA;AA) 0 common in clinvar
Make rs1057520058(-;-)
Make rs1057520058(-;AA)
ReferenceGRCh38.p7 38.3/150
Chromosome17
Position61849226
GeneBRIP1
is asnp
is mentioned by
dbSNPrs1057520058
dbSNP (old)rs1057520058
ClinGenrs1057520058
ebirs1057520058
HLIrs1057520058
Exacrs1057520058
Gnomadrs1057520058
Varsomers1057520058
Maprs1057520058
PheGenIrs1057520058
Biobankrs1057520058
1000 genomesrs1057520058
hgdprs1057520058
ensemblrs1057520058
gopubmedrs1057520058
geneviewrs1057520058
scholarrs1057520058
googlers1057520058
pharmgkbrs1057520058
gwascentralrs1057520058
openSNPrs1057520058
23andMers1057520058
23andMe allrs1057520058
SNPshotrs1057520058
SNPdbers1057520058
MSV3drs1057520058
GWAS Ctlgrs1057520058
Max Magnitude0
ClinVar
Risk rs1057520058(-;-)
Alt rs1057520058(-;-)
Reference Rs1057520058(AA;AA)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene BRIP1
CLNDBN not provided
Reversed 1
HGVS NC_000017.10:g.59926587_59926588delTT
CLNSRC
CLNACC RCV000439831.1,