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rs587777655

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(CTT;CTT) 0 common in clinvar
Make rs587777655(-;-)
Make rs587777655(-;TCT)
Make rs587777655(TCT;TCT)
ReferenceGRCh38 38.1/142
Chromosome11
Position45806304
GeneSLC35C1
is asnp
is mentioned by
dbSNPrs587777655
ebirs587777655
HLIrs587777655
Exacrs587777655
Varsomers587777655
Maprs587777655
PheGenIrs587777655
hapmaprs587777655
1000 genomesrs587777655
hgdprs587777655
ensemblrs587777655
gopubmedrs587777655
geneviewrs587777655
scholarrs587777655
googlers587777655
pharmgkbrs587777655
gwascentralrs587777655
openSNPrs587777655
23andMers587777655
23andMe allrs587777655
SNP Nexus

SNPshotrs587777655
SNPdbers587777655
MSV3drs587777655
GWAS Ctlgrs587777655
Max Magnitude0
ClinVar
Risk rs587777655(;)
Alt rs587777655(;)
Reference rs587777655(CTT;CTT)
Significance Other
Disease Congenital disorder of glycosylation type 2C
Variation info
Gene SLC35C1
CLNDBN Congenital disorder of glycosylation type 2C
Reversed 0
HGVS NC_000011.9:g.45827855_45827857delTCT
CLNSRC OMIM Allelic Variant
CLNACC RCV000133551.4,