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rs752366963

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs752366963(G;G)
Make rs752366963(G;T)
ReferenceGRCh38.p2 38.2/147
Chromosome20
Position18548646
GeneSEC23B
is asnp
is mentioned by
dbSNPrs752366963
ebirs752366963
HLIrs752366963
Exacrs752366963
Varsomers752366963
Maprs752366963
PheGenIrs752366963
hapmaprs752366963
1000 genomesrs752366963
hgdprs752366963
ensemblrs752366963
gopubmedrs752366963
geneviewrs752366963
scholarrs752366963
googlers752366963
pharmgkbrs752366963
gwascentralrs752366963
openSNPrs752366963
23andMers752366963
23andMe allrs752366963
SNP Nexus

SNPshotrs752366963
SNPdbers752366963
MSV3drs752366963
GWAS Ctlgrs752366963
Max Magnitude0
ClinVar
Risk rs752366963(G;G)
Alt rs752366963(G;G)
Reference rs752366963(T;T)
Significance Pathogenic
Disease Cowden syndrome 7
Variation info
Gene SEC23B
CLNDBN Cowden syndrome 7
Reversed 0
HGVS NC_000020.10:g.18529290T>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000210069.1,