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rs202155613

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
(C;T) 6 BRCA2 variant considered pathogenic for breast cancer
Make rs202155613(C;G)
Make rs202155613(G;G)
ReferenceGRCh38.p7 38.3/149
Chromosome13
Position32379902
GeneBRCA2
is asnp
is mentioned by
dbSNPrs202155613
dbSNP (classic)rs202155613
ClinGenrs202155613
ebirs202155613
HLIrs202155613
Exacrs202155613
Gnomadrs202155613
Varsomers202155613
LitVarrs202155613
Maprs202155613
PheGenIrs202155613
Biobankrs202155613
1000 genomesrs202155613
hgdprs202155613
ensemblrs202155613
geneviewrs202155613
scholarrs202155613
googlers202155613
pharmgkbrs202155613
gwascentralrs202155613
openSNPrs202155613
23andMers202155613
23andMe allrs202155613
SNPshotrs202155613
SNPdbers202155613
MSV3drs202155613
GWAS Ctlgrs202155613
Max Magnitude6
ClinVar
Risk rs202155613(A;A) rs202155613(G;G) rs202155613(T;T)
Alt rs202155613(A;A) rs202155613(G;G) rs202155613(T;T)
Reference Rs202155613(C;C)
Significance Other
Disease Hereditary cancer-predisposing syndrome Breast-ovarian cancer not specified Hereditary breast and ovarian cancer syndrome Fanconi anemia not provided
Variation info
Gene BRCA2
CLNDBN Hereditary cancer-predisposing syndrome Breast-ovarian cancer, familial 2 not specified Hereditary breast and ovarian cancer syndrome Fanconi anemia not provided
Reversed 0
HGVS NC_000013.10:g.32954039C>A; NC_000013.10:g.32954039C>G; NC_000013.10:g.32954039C>T
CLNSRC Illumina
CLNACC RCV000164930.1, RCV000031795.4, RCV000074559.4, RCV000223314.1, RCV000289162.1, RCV000344086.1, RCV000257850.2, RCV000481378.1,