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rs771237928

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs771237928(-;-)
Make rs771237928(-;G)
Make rs771237928(G;G)
ReferenceGRCh38.p2 38.2/147
Chromosome1
Position119915812
GeneNOTCH2
is asnp
is mentioned by
dbSNPrs771237928
ebirs771237928
HLIrs771237928
Exacrs771237928
Varsomers771237928
Maprs771237928
PheGenIrs771237928
hapmaprs771237928
1000 genomesrs771237928
hgdprs771237928
ensemblrs771237928
gopubmedrs771237928
geneviewrs771237928
scholarrs771237928
googlers771237928
pharmgkbrs771237928
gwascentralrs771237928
openSNPrs771237928
23andMers771237928
23andMe allrs771237928
SNP Nexus

SNPshotrs771237928
SNPdbers771237928
MSV3drs771237928
GWAS Ctlgrs771237928
Max Magnitude0
ClinVar
Risk rs771237928(G;G)
Alt rs771237928(G;G)
Reference rs771237928(;)
Significance Pathogenic
Disease Monoclonal B-Cell Lymphocytosis
Variation info
Gene NOTCH2
CLNDBN Monoclonal B-Cell Lymphocytosis
Reversed 0
HGVS NC_000001.10:g.120458436dupG
CLNSRC
CLNACC RCV000208622.1,