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rs587777216

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs587777216(C;C)
Make rs587777216(C;T)
ReferenceGRCh38 38.1/142
Chromosome11
Position125618475
GeneSTT3A
is asnp
is mentioned by
dbSNPrs587777216
ebirs587777216
HLIrs587777216
Exacrs587777216
Varsomers587777216
Maprs587777216
PheGenIrs587777216
hapmaprs587777216
1000 genomesrs587777216
hgdprs587777216
ensemblrs587777216
gopubmedrs587777216
geneviewrs587777216
scholarrs587777216
googlers587777216
pharmgkbrs587777216
gwascentralrs587777216
openSNPrs587777216
23andMers587777216
23andMe allrs587777216
SNP Nexus

SNPshotrs587777216
SNPdbers587777216
MSV3drs587777216
GWAS Ctlgrs587777216
Max Magnitude0
ClinVar
Risk rs587777216(C;C)
Alt rs587777216(C;C)
Reference rs587777216(T;T)
Significance Pathogenic
Disease Congenital disorder of glycosylation type 1w
Variation info
Gene STT3A
CLNDBN Congenital disorder of glycosylation type 1w
Reversed 0
HGVS NC_000011.9:g.125488370T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000088679.2,