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rs878853111

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs878853111(A;A)
Make rs878853111(A;T)
ReferenceGRCh38.p2 38.2/147
Chromosome5
Position177257103
GeneNSD1
is asnp
is mentioned by
dbSNPrs878853111
ebirs878853111
HLIrs878853111
Exacrs878853111
Varsomers878853111
Maprs878853111
PheGenIrs878853111
hapmaprs878853111
1000 genomesrs878853111
hgdprs878853111
ensemblrs878853111
gopubmedrs878853111
geneviewrs878853111
scholarrs878853111
googlers878853111
pharmgkbrs878853111
gwascentralrs878853111
openSNPrs878853111
23andMers878853111
23andMe allrs878853111
SNP Nexus

SNPshotrs878853111
SNPdbers878853111
MSV3drs878853111
GWAS Ctlgrs878853111
Max Magnitude0
ClinVar
Risk rs878853111(A;A)
Alt rs878853111(A;A)
Reference rs878853111(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene NSD1
CLNDBN not provided
Reversed 0
HGVS NC_000005.9:g.176684104T>A
CLNSRC
CLNACC RCV000224424.1,