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rs1057517566

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(AA;AA) 0 common in clinvar
Make rs1057517566(-;-)
Make rs1057517566(-;AA)
ReferenceGRCh38.p7 38.3/150
Chromosome13
Position32337431
GeneBRCA2
is asnp
is mentioned by
dbSNPrs1057517566
dbSNP (old)rs1057517566
ClinGenrs1057517566
ebirs1057517566
HLIrs1057517566
Exacrs1057517566
Gnomadrs1057517566
Varsomers1057517566
Maprs1057517566
PheGenIrs1057517566
Biobankrs1057517566
1000 genomesrs1057517566
hgdprs1057517566
ensemblrs1057517566
gopubmedrs1057517566
geneviewrs1057517566
scholarrs1057517566
googlers1057517566
pharmgkbrs1057517566
gwascentralrs1057517566
openSNPrs1057517566
23andMers1057517566
23andMe allrs1057517566
SNPshotrs1057517566
SNPdbers1057517566
MSV3drs1057517566
GWAS Ctlgrs1057517566
Max Magnitude0
ClinVar
Risk rs1057517566(-;-)
Alt rs1057517566(-;-)
Reference Rs1057517566(AA;AA)
Significance Probable-Pathogenic
Disease Breast-ovarian cancer
Variation info
Gene BRCA2
CLNDBN Breast-ovarian cancer, familial 2
Reversed 0
HGVS NC_000013.10:g.32911568_32911569delAA
CLNSRC
CLNACC RCV000409605.1,