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rs727504145

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs727504145(C;T)
Make rs727504145(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome20
Position18542380
GeneSEC23B
is asnp
is mentioned by
dbSNPrs727504145
ebirs727504145
HLIrs727504145
Exacrs727504145
Varsomers727504145
Maprs727504145
PheGenIrs727504145
hapmaprs727504145
1000 genomesrs727504145
hgdprs727504145
ensemblrs727504145
gopubmedrs727504145
geneviewrs727504145
scholarrs727504145
googlers727504145
pharmgkbrs727504145
gwascentralrs727504145
openSNPrs727504145
23andMers727504145
23andMe allrs727504145
SNP Nexus

SNPshotrs727504145
SNPdbers727504145
MSV3drs727504145
GWAS Ctlgrs727504145
Max Magnitude0
ClinVar
Risk rs727504145(T;T)
Alt rs727504145(T;T)
Reference rs727504145(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene SEC23B
CLNDBN not provided
Reversed 0
HGVS NC_000020.10:g.18523024C>T
CLNSRC HGMD
CLNACC RCV000153928.3,