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rs36023150

From SNPedia

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Geno Mag Summary
(G;G) 0 common in clinvar
Make rs36023150(G;T)
Make rs36023150(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome20
Position18524556
GeneSEC23B
is asnp
is mentioned by
dbSNPrs36023150
ebirs36023150
HLIrs36023150
Exacrs36023150
Varsomers36023150
Maprs36023150
PheGenIrs36023150
hapmaprs36023150
1000 genomesrs36023150
hgdprs36023150
ensemblrs36023150
gopubmedrs36023150
geneviewrs36023150
scholarrs36023150
googlers36023150
pharmgkbrs36023150
gwascentralrs36023150
openSNPrs36023150
23andMers36023150
23andMe allrs36023150
SNP Nexus

SNPshotrs36023150
SNPdbers36023150
MSV3drs36023150
GWAS Ctlgrs36023150
Max Magnitude0
ClinVar
Risk rs36023150(T;T)
Alt rs36023150(T;T)
Reference rs36023150(G;G)
Significance Pathogenic
Disease not specified Cowden syndrome 7
Variation info
Gene SEC23B
CLNDBN not specified Cowden syndrome 7
Reversed 0
HGVS NC_000020.10:g.18505200G>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000081408.4, RCV000210063.1,