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rs782357237

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs782357237(-;G)
Make rs782357237(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position149923867
GeneSF3B4
is asnp
is mentioned by
dbSNPrs782357237
ClinGenrs782357237
ebirs782357237
HLIrs782357237
Exacrs782357237
Varsomers782357237
Maprs782357237
PheGenIrs782357237
hapmaprs782357237
1000 genomesrs782357237
hgdprs782357237
ensemblrs782357237
gopubmedrs782357237
geneviewrs782357237
scholarrs782357237
googlers782357237
pharmgkbrs782357237
gwascentralrs782357237
openSNPrs782357237
23andMers782357237
23andMe allrs782357237
SNP Nexus

SNPshotrs782357237
SNPdbers782357237
MSV3drs782357237
GWAS Ctlgrs782357237
Max Magnitude0
ClinVar
Risk rs782357237(G;G)
Alt rs782357237(G;G)
Reference Rs782357237(-;-)
Significance Pathogenic
Disease Nager syndrome
Variation info
Gene SF3B4
CLNDBN Nager syndrome
Reversed 0
HGVS NC_000001.10:g.149895760dupG
CLNSRC
CLNACC RCV000190851.1,