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rs1057517595

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(TG;TG) 0 common in clinvar
Make rs1057517595(-;-)
Make rs1057517595(-;GT)
Make rs1057517595(GT;GT)
ReferenceGRCh38.p7 38.3/150
Chromosome13
Position32339842
GeneBRCA2
is asnp
is mentioned by
dbSNPrs1057517595
dbSNP (classic)rs1057517595
ClinGenrs1057517595
ebirs1057517595
HLIrs1057517595
Exacrs1057517595
Gnomadrs1057517595
Varsomers1057517595
LitVarrs1057517595
Maprs1057517595
PheGenIrs1057517595
Biobankrs1057517595
1000 genomesrs1057517595
hgdprs1057517595
ensemblrs1057517595
geneviewrs1057517595
scholarrs1057517595
googlers1057517595
pharmgkbrs1057517595
gwascentralrs1057517595
openSNPrs1057517595
23andMers1057517595
23andMe allrs1057517595
SNPshotrs1057517595
SNPdbers1057517595
MSV3drs1057517595
GWAS Ctlgrs1057517595
Max Magnitude0
ClinVar
Risk rs1057517595(-;-)
Alt rs1057517595(-;-)
Reference Rs1057517595(TG;TG)
Significance Probable-Pathogenic
Disease Breast-ovarian cancer
Variation info
Gene BRCA2
CLNDBN Breast-ovarian cancer, familial 2
Reversed 0
HGVS NC_000013.10:g.32913979_32913980delGT
CLNSRC
CLNACC RCV000409051.1,