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rs1057517636

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1057517636(A;T)
Make rs1057517636(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome13
Position32338829
GeneBRCA2
is asnp
is mentioned by
dbSNPrs1057517636
dbSNP (old)rs1057517636
ClinGenrs1057517636
ebirs1057517636
HLIrs1057517636
Exacrs1057517636
Gnomadrs1057517636
Varsomers1057517636
LitVarrs1057517636
Maprs1057517636
PheGenIrs1057517636
Biobankrs1057517636
1000 genomesrs1057517636
hgdprs1057517636
ensemblrs1057517636
gopubmedrs1057517636
geneviewrs1057517636
scholarrs1057517636
googlers1057517636
pharmgkbrs1057517636
gwascentralrs1057517636
openSNPrs1057517636
23andMers1057517636
23andMe allrs1057517636
SNPshotrs1057517636
SNPdbers1057517636
MSV3drs1057517636
GWAS Ctlgrs1057517636
Max Magnitude0
ClinVar
Risk rs1057517636(T;T)
Alt rs1057517636(T;T)
Reference Rs1057517636(A;A)
Significance Probable-Pathogenic
Disease Breast-ovarian cancer
Variation info
Gene BRCA2
CLNDBN Breast-ovarian cancer, familial 2
Reversed 0
HGVS NC_000013.10:g.32912966A>T
CLNSRC
CLNACC RCV000411097.1,