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rs1057518637

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057518637(C;T)
Make rs1057518637(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome13
Position32336621
GeneBRCA2
is asnp
is mentioned by
dbSNPrs1057518637
dbSNP (old)rs1057518637
ClinGenrs1057518637
ebirs1057518637
HLIrs1057518637
Exacrs1057518637
Gnomadrs1057518637
Varsomers1057518637
LitVarrs1057518637
Maprs1057518637
PheGenIrs1057518637
Biobankrs1057518637
1000 genomesrs1057518637
hgdprs1057518637
ensemblrs1057518637
gopubmedrs1057518637
geneviewrs1057518637
scholarrs1057518637
googlers1057518637
pharmgkbrs1057518637
gwascentralrs1057518637
openSNPrs1057518637
23andMers1057518637
23andMe allrs1057518637
SNPshotrs1057518637
SNPdbers1057518637
MSV3drs1057518637
GWAS Ctlgrs1057518637
Max Magnitude0
ClinVar
Risk rs1057518637(T;T)
Alt rs1057518637(T;T)
Reference Rs1057518637(C;C)
Significance Pathogenic
Disease Neoplasm of breast
Variation info
Gene BRCA2
CLNDBN Neoplasm of breast
Reversed 0
HGVS NC_000013.10:g.32910758C>T
CLNSRC
CLNACC RCV000414647.1,