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rs786201950

From SNPedia

Orientationplus
Geno Mag Summary
(AG;AG) 0 common in clinvar
Make rs786201950(-;-)
Make rs786201950(-;GA)
Make rs786201950(GA;GA)
ReferenceGRCh38.p2 38.2/146
Chromosome13
Position32332786
GeneBRCA2
is asnp
is mentioned by
dbSNPrs786201950
ebirs786201950
HLIrs786201950
Exacrs786201950
Varsomers786201950
Maprs786201950
PheGenIrs786201950
hapmaprs786201950
1000 genomesrs786201950
hgdprs786201950
ensemblrs786201950
gopubmedrs786201950
geneviewrs786201950
scholarrs786201950
googlers786201950
pharmgkbrs786201950
gwascentralrs786201950
openSNPrs786201950
23andMers786201950
23andMe allrs786201950
SNP Nexus

SNPshotrs786201950
SNPdbers786201950
MSV3drs786201950
GWAS Ctlgrs786201950
Max Magnitude0
ClinVar
Risk rs786201950(;)
Alt rs786201950(;)
Reference rs786201950(AG;AG)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene BRCA2
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000013.10:g.32906923_32906924delGA
CLNSRC
CLNACC RCV000164498.1,