Have questions? Visit https://www.reddit.com/r/SNPedia

rs797045122

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs797045122(-;-)
Make rs797045122(-;C)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position149923585
GeneSF3B4
is asnp
is mentioned by
dbSNPrs797045122
dbSNP (classic)rs797045122
ClinGenrs797045122
ebirs797045122
HLIrs797045122
Exacrs797045122
Gnomadrs797045122
Varsomers797045122
LitVarrs797045122
Maprs797045122
PheGenIrs797045122
Biobankrs797045122
1000 genomesrs797045122
hgdprs797045122
ensemblrs797045122
geneviewrs797045122
scholarrs797045122
googlers797045122
pharmgkbrs797045122
gwascentralrs797045122
openSNPrs797045122
23andMers797045122
SNPshotrs797045122
SNPdbers797045122
MSV3drs797045122
GWAS Ctlgrs797045122
Max Magnitude0
ClinVar
Risk rs797045122(-;-)
Alt rs797045122(-;-)
Reference Rs797045122(C;C)
Significance Pathogenic
Disease Nager syndrome
Variation info
Gene SF3B4
CLNDBN Nager syndrome
Reversed 1
HGVS NC_000001.10:g.149895477delG
CLNSRC
CLNACC RCV000190848.1,