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rs10492396

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs10492396(A;A)
Make rs10492396(A;G)
ReferenceGRCh38 38.1/142
Chromosome13
Position32384750
GeneBRCA2
is asnp
is mentioned by
dbSNPrs10492396
ebirs10492396
HLIrs10492396
Exacrs10492396
Varsomers10492396
Maprs10492396
PheGenIrs10492396
hapmaprs10492396
1000 genomesrs10492396
hgdprs10492396
ensemblrs10492396
gopubmedrs10492396
geneviewrs10492396
scholarrs10492396
googlers10492396
pharmgkbrs10492396
gwascentralrs10492396
openSNPrs10492396
23andMers10492396
23andMe allrs10492396
SNP Nexus

SNPshotrs10492396
SNPdbers10492396
MSV3drs10492396
GWAS Ctlgrs10492396
Max Magnitude0
? (A;A) (A;G) (G;G) 28

[PMID 25243787] Genetic variants in fanconi anemia pathway genes BRCA2 and FANCA predict melanoma survival


ClinVar
Risk rs10492396(A;A)
Alt rs10492396(A;A)
Reference rs10492396(G;G)
Significance Non-pathogenic
Disease Breast-ovarian cancer
Variation info
Gene BRCA2
CLNDBN Breast-ovarian cancer, familial 2
Reversed 0
HGVS NC_000013.10:g.32958887G>A
CLNSRC
CLNACC RCV000191814.1,