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rs206118

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs206118(C;C)
Make rs206118(C;T)
ReferenceGRCh38 38.1/142
Chromosome13
Position32315655
GeneBRCA2
is asnp
is mentioned by
dbSNPrs206118
ebirs206118
HLIrs206118
Exacrs206118
Varsomers206118
Maprs206118
PheGenIrs206118
hapmaprs206118
1000 genomesrs206118
hgdprs206118
ensemblrs206118
gopubmedrs206118
geneviewrs206118
scholarrs206118
googlers206118
pharmgkbrs206118
gwascentralrs206118
openSNPrs206118
23andMers206118
23andMe allrs206118
SNP Nexus

SNPshotrs206118
SNPdbers206118
MSV3drs206118
GWAS Ctlgrs206118
Max Magnitude0
? (C;C) (C;T) (T;T) 28
[PMID 25243787OA-icon.png] Genetic variants in fanconi anemia pathway genes BRCA2 and FANCA predict melanoma survival


ClinVar
Risk rs206118(C;C)
Alt rs206118(C;C)
Reference rs206118(T;T)
Significance Non-pathogenic
Disease Breast-ovarian cancer
Variation info
Gene BRCA2
CLNDBN Breast-ovarian cancer, familial 2
Reversed 1
HGVS NC_000013.10:g.32889792A>G
CLNSRC
CLNACC RCV000191546.1,