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rs797045955

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs797045955(G;T)
Make rs797045955(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position149926889
GeneSF3B4
is asnp
is mentioned by
dbSNPrs797045955
ebirs797045955
HLIrs797045955
Exacrs797045955
Varsomers797045955
Maprs797045955
PheGenIrs797045955
hapmaprs797045955
1000 genomesrs797045955
hgdprs797045955
ensemblrs797045955
gopubmedrs797045955
geneviewrs797045955
scholarrs797045955
googlers797045955
pharmgkbrs797045955
gwascentralrs797045955
openSNPrs797045955
23andMers797045955
23andMe allrs797045955
SNP Nexus

SNPshotrs797045955
SNPdbers797045955
MSV3drs797045955
GWAS Ctlgrs797045955
Max Magnitude0
ClinVar
Risk rs797045955(T;T)
Alt rs797045955(T;T)
Reference rs797045955(G;G)
Significance Pathogenic
Disease Nager syndrome
Variation info
Gene SF3B4
CLNDBN Nager syndrome
Reversed 1
HGVS NC_000001.10:g.149898781C>A
CLNSRC
CLNACC RCV000193888.1,