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rs398124227

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs398124227(A;A)
Make rs398124227(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome20
Position18525840
GeneSEC23B
is asnp
is mentioned by
dbSNPrs398124227
ebirs398124227
HLIrs398124227
Exacrs398124227
Varsomers398124227
Maprs398124227
PheGenIrs398124227
hapmaprs398124227
1000 genomesrs398124227
hgdprs398124227
ensemblrs398124227
gopubmedrs398124227
geneviewrs398124227
scholarrs398124227
googlers398124227
pharmgkbrs398124227
gwascentralrs398124227
openSNPrs398124227
23andMers398124227
23andMe allrs398124227
SNP Nexus

SNPshotrs398124227
SNPdbers398124227
MSV3drs398124227
GWAS Ctlgrs398124227
Max Magnitude0
ClinVar
Risk rs398124227(A;A)
Alt rs398124227(A;A)
Reference rs398124227(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SEC23B
CLNDBN not provided
Reversed 0
HGVS NC_000020.10:g.18506484G>A
CLNSRC HGMD
CLNACC RCV000081410.4,