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

rs121918225

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121918225(C;T)
Make rs121918225(T;T)
ReferenceGRCh38 38.1/141
Chromosome20
Position18526508
GeneSEC23B
is asnp
is mentioned by
dbSNPrs121918225
ebirs121918225
HLIrs121918225
Exacrs121918225
Varsomers121918225
Maprs121918225
PheGenIrs121918225
hapmaprs121918225
1000 genomesrs121918225
hgdprs121918225
ensemblrs121918225
gopubmedrs121918225
geneviewrs121918225
scholarrs121918225
googlers121918225
pharmgkbrs121918225
gwascentralrs121918225
openSNPrs121918225
23andMers121918225
23andMe allrs121918225
SNP Nexus

SNPshotrs121918225
SNPdbers121918225
MSV3drs121918225
GWAS Ctlgrs121918225
Max Magnitude0
OMIM610512
Desc
Variant0005
Relatedalso
ClinVar
Risk rs121918225(T;T)
Alt rs121918225(T;T)
Reference rs121918225(C;C)
Significance Pathogenic
Disease Congenital dyserythropoietic anemia
Variation info
Gene SEC23B
CLNDBN Congenital dyserythropoietic anemia, type II
Reversed 0
HGVS NC_000020.10:g.18507152C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000001285.4,