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rs751828447

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs751828447(C;T)
Make rs751828447(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position45811112
GeneLOC105376659, SLC35C1
is asnp
is mentioned by
dbSNPrs751828447
ebirs751828447
HLIrs751828447
Exacrs751828447
Varsomers751828447
Maprs751828447
PheGenIrs751828447
hapmaprs751828447
1000 genomesrs751828447
hgdprs751828447
ensemblrs751828447
gopubmedrs751828447
geneviewrs751828447
scholarrs751828447
googlers751828447
pharmgkbrs751828447
gwascentralrs751828447
openSNPrs751828447
23andMers751828447
23andMe allrs751828447
SNP Nexus

SNPshotrs751828447
SNPdbers751828447
MSV3drs751828447
GWAS Ctlgrs751828447
Max Magnitude0
ClinVar
Risk rs751828447(T;T)
Alt rs751828447(T;T)
Reference rs751828447(C;C)
Significance Probable-Pathogenic
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.45832663C>T
CLNSRC
CLNACC RCV000197101.1,