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rs1057518638

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1057518638(A;A)
Make rs1057518638(A;T)
ReferenceGRCh38.p7 38.3/150
Chromosome13
Position32339317
GeneBRCA2
is asnp
is mentioned by
dbSNPrs1057518638
dbSNP (old)rs1057518638
ClinGenrs1057518638
ebirs1057518638
HLIrs1057518638
Exacrs1057518638
Gnomadrs1057518638
Varsomers1057518638
LitVarrs1057518638
Maprs1057518638
PheGenIrs1057518638
Biobankrs1057518638
1000 genomesrs1057518638
hgdprs1057518638
ensemblrs1057518638
gopubmedrs1057518638
geneviewrs1057518638
scholarrs1057518638
googlers1057518638
pharmgkbrs1057518638
gwascentralrs1057518638
openSNPrs1057518638
23andMers1057518638
23andMe allrs1057518638
SNPshotrs1057518638
SNPdbers1057518638
MSV3drs1057518638
GWAS Ctlgrs1057518638
Max Magnitude0
ClinVar
Risk rs1057518638(A;A)
Alt rs1057518638(A;A)
Reference Rs1057518638(T;T)
Significance Pathogenic
Disease Neoplasm of breast
Variation info
Gene BRCA2
CLNDBN Neoplasm of breast
Reversed 0
HGVS NC_000013.10:g.32913454T>A
CLNSRC
CLNACC RCV000414119.1,