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rs878855228

From SNPedia

Orientationplus
Geno Mag Summary
(AG;AG) 0 common in clinvar
Make rs878855228(-;-)
Make rs878855228(-;AG)
ReferenceGRCh38.p2 38.2/147
Chromosome15
Position38351480
GeneSPRED1
is asnp
is mentioned by
dbSNPrs878855228
ebirs878855228
HLIrs878855228
Exacrs878855228
Varsomers878855228
Maprs878855228
PheGenIrs878855228
hapmaprs878855228
1000 genomesrs878855228
hgdprs878855228
ensemblrs878855228
gopubmedrs878855228
geneviewrs878855228
scholarrs878855228
googlers878855228
pharmgkbrs878855228
gwascentralrs878855228
openSNPrs878855228
23andMers878855228
23andMe allrs878855228
SNP Nexus

SNPshotrs878855228
SNPdbers878855228
MSV3drs878855228
GWAS Ctlgrs878855228
Max Magnitude0
ClinVar
Risk rs878855228(;)
Alt rs878855228(;)
Reference rs878855228(AG;AG)
Significance Pathogenic
Disease Legius syndrome
Variation info
Gene SPRED1
CLNDBN Legius syndrome
Reversed 0
HGVS NC_000015.9:g.38643681_38643682delAG
CLNSRC
CLNACC RCV000226597.1,