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rs794726683

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs794726683(-;-)
Make rs794726683(-;G)
Make rs794726683(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome3
Position47002756
GeneNBEAL2
is asnp
is mentioned by
dbSNPrs794726683
ebirs794726683
HLIrs794726683
Exacrs794726683
Varsomers794726683
Maprs794726683
PheGenIrs794726683
hapmaprs794726683
1000 genomesrs794726683
hgdprs794726683
ensemblrs794726683
gopubmedrs794726683
geneviewrs794726683
scholarrs794726683
googlers794726683
pharmgkbrs794726683
gwascentralrs794726683
openSNPrs794726683
23andMers794726683
23andMe allrs794726683
SNP Nexus

SNPshotrs794726683
SNPdbers794726683
MSV3drs794726683
GWAS Ctlgrs794726683
Max Magnitude0
ClinVar
Risk rs794726683(G;G)
Alt rs794726683(G;G)
Reference rs794726683(;)
Significance Pathogenic
Disease Gray platelet syndrome
Variation info
Gene NBEAL2
CLNDBN Gray platelet syndrome
Reversed 0
HGVS NC_000003.11:g.47044246dupG
CLNSRC OMIM Allelic Variant
CLNACC RCV000024118.3,