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rs1057517865

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1057517865(A;T)
Make rs1057517865(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome13
Position32371025
GeneBRCA2
is asnp
is mentioned by
dbSNPrs1057517865
dbSNP (old)rs1057517865
ClinGenrs1057517865
ebirs1057517865
HLIrs1057517865
Exacrs1057517865
Gnomadrs1057517865
Varsomers1057517865
LitVarrs1057517865
Maprs1057517865
PheGenIrs1057517865
Biobankrs1057517865
1000 genomesrs1057517865
hgdprs1057517865
ensemblrs1057517865
gopubmedrs1057517865
geneviewrs1057517865
scholarrs1057517865
googlers1057517865
pharmgkbrs1057517865
gwascentralrs1057517865
openSNPrs1057517865
23andMers1057517865
23andMe allrs1057517865
SNPshotrs1057517865
SNPdbers1057517865
MSV3drs1057517865
GWAS Ctlgrs1057517865
Max Magnitude0
ClinVar
Risk rs1057517865(T;T)
Alt rs1057517865(T;T)
Reference Rs1057517865(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene BRCA2
CLNDBN not provided
Reversed 0
HGVS NC_000013.10:g.32945162A>T
CLNSRC
CLNACC RCV000414464.1,