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rs1057521184

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057521184(G;T)
Make rs1057521184(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome13
Position32363372
GeneBRCA2
is asnp
is mentioned by
dbSNPrs1057521184
dbSNP (old)rs1057521184
ClinGenrs1057521184
ebirs1057521184
HLIrs1057521184
Exacrs1057521184
Gnomadrs1057521184
Varsomers1057521184
Maprs1057521184
PheGenIrs1057521184
Biobankrs1057521184
1000 genomesrs1057521184
hgdprs1057521184
ensemblrs1057521184
gopubmedrs1057521184
geneviewrs1057521184
scholarrs1057521184
googlers1057521184
pharmgkbrs1057521184
gwascentralrs1057521184
openSNPrs1057521184
23andMers1057521184
23andMe allrs1057521184
SNPshotrs1057521184
SNPdbers1057521184
MSV3drs1057521184
GWAS Ctlgrs1057521184
Max Magnitude0
ClinVar
Risk rs1057521184(T;T)
Alt rs1057521184(T;T)
Reference Rs1057521184(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene BRCA2
CLNDBN not provided
Reversed 0
HGVS NC_000013.10:g.32937509G>T
CLNSRC
CLNACC RCV000417977.1,