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rs786203845

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs786203845(G;T)
Make rs786203845(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome13
Position32336315
GeneBRCA2
is asnp
is mentioned by
dbSNPrs786203845
ebirs786203845
HLIrs786203845
Exacrs786203845
Varsomers786203845
Maprs786203845
PheGenIrs786203845
hapmaprs786203845
1000 genomesrs786203845
hgdprs786203845
ensemblrs786203845
gopubmedrs786203845
geneviewrs786203845
scholarrs786203845
googlers786203845
pharmgkbrs786203845
gwascentralrs786203845
openSNPrs786203845
23andMers786203845
23andMe allrs786203845
SNP Nexus

SNPshotrs786203845
SNPdbers786203845
MSV3drs786203845
GWAS Ctlgrs786203845
Max Magnitude0
ClinVar
Risk rs786203845(T;T)
Alt rs786203845(T;T)
Reference rs786203845(G;G)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene BRCA2
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000013.10:g.32910452G>T
CLNSRC
CLNACC RCV000167330.1,