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rs587777217

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587777217(G;T)
Make rs587777217(T;T)
ReferenceGRCh38 38.1/142
Chromosome3
Position31622328
GeneSTT3B
is asnp
is mentioned by
dbSNPrs587777217
ebirs587777217
HLIrs587777217
Exacrs587777217
Varsomers587777217
Maprs587777217
PheGenIrs587777217
hapmaprs587777217
1000 genomesrs587777217
hgdprs587777217
ensemblrs587777217
gopubmedrs587777217
geneviewrs587777217
scholarrs587777217
googlers587777217
pharmgkbrs587777217
gwascentralrs587777217
openSNPrs587777217
23andMers587777217
23andMe allrs587777217
SNP Nexus

SNPshotrs587777217
SNPdbers587777217
MSV3drs587777217
GWAS Ctlgrs587777217
Max Magnitude0
ClinVar
Risk rs587777217(T;T)
Alt rs587777217(T;T)
Reference rs587777217(G;G)
Significance Pathogenic
Disease Congenital disorder of glycosylation type 1x
Variation info
Gene STT3B
CLNDBN Congenital disorder of glycosylation type 1x
Reversed 0
HGVS NC_000003.11:g.31663820G>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000088685.3,