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rs878855075

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs878855075(-;-)
Make rs878855075(-;GA)
Make rs878855075(GA;GA)
ReferenceGRCh38.p2 38.2/147
Chromosome5
Position177211947
GeneNSD1
is asnp
is mentioned by
dbSNPrs878855075
ebirs878855075
HLIrs878855075
Exacrs878855075
Varsomers878855075
Maprs878855075
PheGenIrs878855075
hapmaprs878855075
1000 genomesrs878855075
hgdprs878855075
ensemblrs878855075
gopubmedrs878855075
geneviewrs878855075
scholarrs878855075
googlers878855075
pharmgkbrs878855075
gwascentralrs878855075
openSNPrs878855075
23andMers878855075
23andMe allrs878855075
SNP Nexus

SNPshotrs878855075
SNPdbers878855075
MSV3drs878855075
GWAS Ctlgrs878855075
Max Magnitude0
ClinVar
Risk rs878855075(GA;GA)
Alt rs878855075(GA;GA)
Reference rs878855075(;)
Significance Pathogenic
Disease Beckwith-Wiedemann syndrome
Variation info
Gene NSD1
CLNDBN Beckwith-Wiedemann syndrome
Reversed 0
HGVS NC_000005.9:g.176638948_176638949insGA
CLNSRC
CLNACC RCV000231883.1,