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rs797045125

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs797045125(A;A)
Make rs797045125(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position149925835
GeneSF3B4
is asnp
is mentioned by
dbSNPrs797045125
ClinGenrs797045125
ebirs797045125
HLIrs797045125
Exacrs797045125
Varsomers797045125
Maprs797045125
PheGenIrs797045125
hapmaprs797045125
1000 genomesrs797045125
hgdprs797045125
ensemblrs797045125
gopubmedrs797045125
geneviewrs797045125
scholarrs797045125
googlers797045125
pharmgkbrs797045125
gwascentralrs797045125
openSNPrs797045125
23andMers797045125
23andMe allrs797045125
SNP Nexus

SNPshotrs797045125
SNPdbers797045125
MSV3drs797045125
GWAS Ctlgrs797045125
Max Magnitude0
ClinVar
Risk rs797045125(A;A)
Alt rs797045125(A;A)
Reference Rs797045125(G;G)
Significance Pathogenic
Disease Nager syndrome
Variation info
Gene SF3B4
CLNDBN Nager syndrome
Reversed 1
HGVS NC_000001.10:g.149897727C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000024347.3,