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rs1057517572

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs1057517572(-;T)
Make rs1057517572(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome13
Position32319317
GeneBRCA2
is asnp
is mentioned by
dbSNPrs1057517572
dbSNP (old)rs1057517572
ClinGenrs1057517572
ebirs1057517572
HLIrs1057517572
Exacrs1057517572
Gnomadrs1057517572
Varsomers1057517572
Maprs1057517572
PheGenIrs1057517572
Biobankrs1057517572
1000 genomesrs1057517572
hgdprs1057517572
ensemblrs1057517572
gopubmedrs1057517572
geneviewrs1057517572
scholarrs1057517572
googlers1057517572
pharmgkbrs1057517572
gwascentralrs1057517572
openSNPrs1057517572
23andMers1057517572
23andMe allrs1057517572
SNPshotrs1057517572
SNPdbers1057517572
MSV3drs1057517572
GWAS Ctlgrs1057517572
Max Magnitude0
ClinVar
Risk rs1057517572(T;T)
Alt rs1057517572(T;T)
Reference Rs1057517572(-;-)
Significance Probable-Pathogenic
Disease Breast-ovarian cancer
Variation info
Gene BRCA2
CLNDBN Breast-ovarian cancer, familial 2
Reversed 0
HGVS NC_000013.10:g.32893454dupT
CLNSRC
CLNACC RCV000412296.1,