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rs797044869

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs797044869(A;A)
Make rs797044869(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position149926919
GeneSF3B4
is asnp
is mentioned by
dbSNPrs797044869
ebirs797044869
HLIrs797044869
Exacrs797044869
Varsomers797044869
Maprs797044869
PheGenIrs797044869
hapmaprs797044869
1000 genomesrs797044869
hgdprs797044869
ensemblrs797044869
gopubmedrs797044869
geneviewrs797044869
scholarrs797044869
googlers797044869
pharmgkbrs797044869
gwascentralrs797044869
openSNPrs797044869
23andMers797044869
23andMe allrs797044869
SNP Nexus

SNPshotrs797044869
SNPdbers797044869
MSV3drs797044869
GWAS Ctlgrs797044869
Max Magnitude0
ClinVar
Risk rs797044869(A;A)
Alt rs797044869(A;A)
Reference rs797044869(G;G)
Significance Pathogenic
Disease Inborn genetic diseases
Variation info
Gene SF3B4
CLNDBN Inborn genetic diseases
Reversed 1
HGVS NC_000001.10:g.149898811C>T
CLNSRC
CLNACC RCV000190676.1,