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rs786203340

From SNPedia

Orientationplus
Geno Mag Summary
(TCAAA;TCAAA) 0 common in clinvar
Make rs786203340(-;-)
Make rs786203340(-;CAAAT)
Make rs786203340(CAAAT;CAAAT)
ReferenceGRCh38.p2 38.2/146
Chromosome13
Position32338566
GeneBRCA2
is asnp
is mentioned by
dbSNPrs786203340
ebirs786203340
HLIrs786203340
Exacrs786203340
Varsomers786203340
Maprs786203340
PheGenIrs786203340
hapmaprs786203340
1000 genomesrs786203340
hgdprs786203340
ensemblrs786203340
gopubmedrs786203340
geneviewrs786203340
scholarrs786203340
googlers786203340
pharmgkbrs786203340
gwascentralrs786203340
openSNPrs786203340
23andMers786203340
23andMe allrs786203340
SNP Nexus

SNPshotrs786203340
SNPdbers786203340
MSV3drs786203340
GWAS Ctlgrs786203340
Max Magnitude0
ClinVar
Risk rs786203340(;)
Alt rs786203340(;)
Reference rs786203340(TCAAA;TCAAA)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene BRCA2
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000013.10:g.32912703_32912707delCAAAT
CLNSRC
CLNACC RCV000166608.1,