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rs1057518635

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(AGAT;AGAT) 0 common in clinvar
Make rs1057518635(-;-)
Make rs1057518635(-;ATAG)
Make rs1057518635(ATAG;ATAG)
ReferenceGRCh38.p7 38.3/150
Chromosome13
Position32340369
GeneBRCA2
is asnp
is mentioned by
dbSNPrs1057518635
dbSNP (old)rs1057518635
ClinGenrs1057518635
ebirs1057518635
HLIrs1057518635
Exacrs1057518635
Gnomadrs1057518635
Varsomers1057518635
Maprs1057518635
PheGenIrs1057518635
Biobankrs1057518635
1000 genomesrs1057518635
hgdprs1057518635
ensemblrs1057518635
gopubmedrs1057518635
geneviewrs1057518635
scholarrs1057518635
googlers1057518635
pharmgkbrs1057518635
gwascentralrs1057518635
openSNPrs1057518635
23andMers1057518635
23andMe allrs1057518635
SNPshotrs1057518635
SNPdbers1057518635
MSV3drs1057518635
GWAS Ctlgrs1057518635
Max Magnitude0
ClinVar
Risk rs1057518635(-;-)
Alt rs1057518635(-;-)
Reference Rs1057518635(AGAT;AGAT)
Significance Pathogenic
Disease Neoplasm of breast not provided
Variation info
Gene BRCA2
CLNDBN Neoplasm of breast not provided
Reversed 0
HGVS NC_000013.10:g.32914506_32914509delATAG
CLNSRC
CLNACC RCV000414026.1, RCV000479529.1,