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rs786202421

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs786202421(C;T)
Make rs786202421(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome13
Position32338601
GeneBRCA2
is asnp
is mentioned by
dbSNPrs786202421
ebirs786202421
HLIrs786202421
Exacrs786202421
Varsomers786202421
Maprs786202421
PheGenIrs786202421
hapmaprs786202421
1000 genomesrs786202421
hgdprs786202421
ensemblrs786202421
gopubmedrs786202421
geneviewrs786202421
scholarrs786202421
googlers786202421
pharmgkbrs786202421
gwascentralrs786202421
openSNPrs786202421
23andMers786202421
23andMe allrs786202421
SNP Nexus

SNPshotrs786202421
SNPdbers786202421
MSV3drs786202421
GWAS Ctlgrs786202421
Max Magnitude0
ClinVar
Risk rs786202421(T;T)
Alt rs786202421(T;T)
Reference rs786202421(C;C)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene BRCA2
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000013.10:g.32912738C>T
CLNSRC
CLNACC RCV000165228.1,