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rs1057520636

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1057520636(A;A)
Make rs1057520636(A;T)
ReferenceGRCh38.p7 38.3/150
Chromosome13
Position32338581
GeneBRCA2
is asnp
is mentioned by
dbSNPrs1057520636
dbSNP (old)rs1057520636
ClinGenrs1057520636
ebirs1057520636
HLIrs1057520636
Exacrs1057520636
Gnomadrs1057520636
Varsomers1057520636
Maprs1057520636
PheGenIrs1057520636
Biobankrs1057520636
1000 genomesrs1057520636
hgdprs1057520636
ensemblrs1057520636
gopubmedrs1057520636
geneviewrs1057520636
scholarrs1057520636
googlers1057520636
pharmgkbrs1057520636
gwascentralrs1057520636
openSNPrs1057520636
23andMers1057520636
23andMe allrs1057520636
SNPshotrs1057520636
SNPdbers1057520636
MSV3drs1057520636
GWAS Ctlgrs1057520636
Max Magnitude0
ClinVar
Risk rs1057520636(A;A)
Alt rs1057520636(A;A)
Reference Rs1057520636(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene BRCA2
CLNDBN not provided
Reversed 0
HGVS NC_000013.10:g.32912718T>A
CLNSRC
CLNACC RCV000435713.1,