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rs398124225

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs398124225(C;T)
Make rs398124225(T;T)
ReferenceGRCh38 38.1/141
Chromosome20
Position18543078
GeneSEC23B
is asnp
is mentioned by
dbSNPrs398124225
ebirs398124225
HLIrs398124225
Exacrs398124225
Varsomers398124225
Maprs398124225
PheGenIrs398124225
hapmaprs398124225
1000 genomesrs398124225
hgdprs398124225
ensemblrs398124225
gopubmedrs398124225
geneviewrs398124225
scholarrs398124225
googlers398124225
pharmgkbrs398124225
gwascentralrs398124225
openSNPrs398124225
23andMers398124225
23andMe allrs398124225
SNP Nexus

SNPshotrs398124225
SNPdbers398124225
MSV3drs398124225
GWAS Ctlgrs398124225
Max Magnitude0
ClinVar
Risk rs398124225(T;T)
Alt rs398124225(T;T)
Reference rs398124225(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene SEC23B
CLNDBN not provided
Reversed 0
HGVS NC_000020.10:g.18523722C>T
CLNSRC HGMD
CLNACC RCV000081403.4,