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rs1057517565

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(TTTC;TTTC) 0 common in clinvar
Make rs1057517565(-;-)
Make rs1057517565(-;TTTC)
ReferenceGRCh38.p7 38.3/150
Chromosome13
Position32338925
GeneBRCA2
is asnp
is mentioned by
dbSNPrs1057517565
dbSNP (old)rs1057517565
ClinGenrs1057517565
ebirs1057517565
HLIrs1057517565
Exacrs1057517565
Gnomadrs1057517565
Varsomers1057517565
Maprs1057517565
PheGenIrs1057517565
Biobankrs1057517565
1000 genomesrs1057517565
hgdprs1057517565
ensemblrs1057517565
gopubmedrs1057517565
geneviewrs1057517565
scholarrs1057517565
googlers1057517565
pharmgkbrs1057517565
gwascentralrs1057517565
openSNPrs1057517565
23andMers1057517565
23andMe allrs1057517565
SNPshotrs1057517565
SNPdbers1057517565
MSV3drs1057517565
GWAS Ctlgrs1057517565
Max Magnitude0
ClinVar
Risk rs1057517565(-;-)
Alt rs1057517565(-;-)
Reference Rs1057517565(TTTC;TTTC)
Significance Probable-Pathogenic
Disease Breast-ovarian cancer
Variation info
Gene BRCA2
CLNDBN Breast-ovarian cancer, familial 2
Reversed 0
HGVS NC_000013.10:g.32913062_32913065delTTTC
CLNSRC
CLNACC RCV000410419.1,