Have questions? Visit https://www.reddit.com/r/SNPedia

rs769366055

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs769366055(C;G)
Make rs769366055(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome1
Position43424324
GeneSZT2
is asnp
is mentioned by
dbSNPrs769366055
dbSNP (classic)rs769366055
ClinGenrs769366055
ebirs769366055
HLIrs769366055
Exacrs769366055
Gnomadrs769366055
Varsomers769366055
LitVarrs769366055
Maprs769366055
PheGenIrs769366055
Biobankrs769366055
1000 genomesrs769366055
hgdprs769366055
ensemblrs769366055
geneviewrs769366055
scholarrs769366055
googlers769366055
pharmgkbrs769366055
gwascentralrs769366055
openSNPrs769366055
23andMers769366055
SNPshotrs769366055
SNPdbers769366055
MSV3drs769366055
GWAS Ctlgrs769366055
Max Magnitude0
ClinVar
Risk rs769366055(G;G)
Alt rs769366055(G;G)
Reference Rs769366055(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene SZT2
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.43889995C>G
CLNSRC
CLNACC RCV000494105.1,