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

rs398124226

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs398124226(A;A)
Make rs398124226(A;G)
ReferenceGRCh38 38.1/141
Chromosome20
Position18525021
GeneSEC23B
is asnp
is mentioned by
dbSNPrs398124226
ebirs398124226
HLIrs398124226
Exacrs398124226
Varsomers398124226
Maprs398124226
PheGenIrs398124226
hapmaprs398124226
1000 genomesrs398124226
hgdprs398124226
ensemblrs398124226
gopubmedrs398124226
geneviewrs398124226
scholarrs398124226
googlers398124226
pharmgkbrs398124226
gwascentralrs398124226
openSNPrs398124226
23andMers398124226
23andMe allrs398124226
SNP Nexus

SNPshotrs398124226
SNPdbers398124226
MSV3drs398124226
GWAS Ctlgrs398124226
Max Magnitude0
ClinVar
Risk rs398124226(A,C;A,C)
Alt rs398124226(A,C;A,C)
Reference rs398124226(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene SEC23B
CLNDBN not provided
Reversed 0
HGVS NC_000020.10:g.18505665G>A
CLNSRC HGMD
CLNACC RCV000081409.4,