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rs797045133

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs797045133(A;A)
Make rs797045133(A;C)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position149926630
GeneSF3B4
is asnp
is mentioned by
dbSNPrs797045133
ebirs797045133
HLIrs797045133
Exacrs797045133
Varsomers797045133
Maprs797045133
PheGenIrs797045133
hapmaprs797045133
1000 genomesrs797045133
hgdprs797045133
ensemblrs797045133
gopubmedrs797045133
geneviewrs797045133
scholarrs797045133
googlers797045133
pharmgkbrs797045133
gwascentralrs797045133
openSNPrs797045133
23andMers797045133
23andMe allrs797045133
SNP Nexus

SNPshotrs797045133
SNPdbers797045133
MSV3drs797045133
GWAS Ctlgrs797045133
Max Magnitude0
ClinVar
Risk rs797045133(A;A)
Alt rs797045133(A;A)
Reference rs797045133(C;C)
Significance Pathogenic
Disease Nager syndrome
Variation info
Gene SF3B4
CLNDBN Nager syndrome
Reversed 1
HGVS NC_000001.10:g.149898522G>T
CLNSRC
CLNACC RCV000190860.1,