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rs786202160

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs786202160(-;-)
Make rs786202160(-;G)
ReferenceGRCh38.p2 38.2/146
Chromosome13
Position32337720
GeneBRCA2
is asnp
is mentioned by
dbSNPrs786202160
ebirs786202160
HLIrs786202160
Exacrs786202160
Varsomers786202160
Maprs786202160
PheGenIrs786202160
hapmaprs786202160
1000 genomesrs786202160
hgdprs786202160
ensemblrs786202160
gopubmedrs786202160
geneviewrs786202160
scholarrs786202160
googlers786202160
pharmgkbrs786202160
gwascentralrs786202160
openSNPrs786202160
23andMers786202160
23andMe allrs786202160
SNP Nexus

SNPshotrs786202160
SNPdbers786202160
MSV3drs786202160
GWAS Ctlgrs786202160
Max Magnitude0
ClinVar
Risk rs786202160(;)
Alt rs786202160(;)
Reference rs786202160(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.32911857delG
CLNSRC
CLNACC RCV000164839.1,