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rs797045132

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs797045132(C;T)
Make rs797045132(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position149926457
GeneSF3B4
is asnp
is mentioned by
dbSNPrs797045132
ebirs797045132
HLIrs797045132
Exacrs797045132
Varsomers797045132
Maprs797045132
PheGenIrs797045132
hapmaprs797045132
1000 genomesrs797045132
hgdprs797045132
ensemblrs797045132
gopubmedrs797045132
geneviewrs797045132
scholarrs797045132
googlers797045132
pharmgkbrs797045132
gwascentralrs797045132
openSNPrs797045132
23andMers797045132
23andMe allrs797045132
SNP Nexus

SNPshotrs797045132
SNPdbers797045132
MSV3drs797045132
GWAS Ctlgrs797045132
Max Magnitude0
ClinVar
Risk rs797045132(T;T)
Alt rs797045132(T;T)
Reference rs797045132(C;C)
Significance Pathogenic
Disease Nager syndrome
Variation info
Gene SF3B4
CLNDBN Nager syndrome
Reversed 1
HGVS NC_000001.10:g.149898349G>A
CLNSRC
CLNACC RCV000190859.1,