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rs119103237

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs119103237(C;C)
Make rs119103237(C;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position184245798
GeneALG3
is asnp
is mentioned by
dbSNPrs119103237
ebirs119103237
HLIrs119103237
Exacrs119103237
Varsomers119103237
Maprs119103237
PheGenIrs119103237
hapmaprs119103237
1000 genomesrs119103237
hgdprs119103237
ensemblrs119103237
gopubmedrs119103237
geneviewrs119103237
scholarrs119103237
googlers119103237
pharmgkbrs119103237
gwascentralrs119103237
openSNPrs119103237
23andMers119103237
23andMe allrs119103237
SNP Nexus

SNPshotrs119103237
SNPdbers119103237
MSV3drs119103237
GWAS Ctlgrs119103237
Max Magnitude0
OMIM608750
Desc
Variant0004
Relatedalso
ClinVar
Risk rs119103237(C;C)
Alt rs119103237(C;C)
Reference rs119103237(T;T)
Significance Pathogenic
Disease Congenital disorder of glycosylation type 1D
Variation info
Gene ALG3
CLNDBN Congenital disorder of glycosylation type 1D
Reversed 1
HGVS NC_000003.11:g.183963586A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000002212.3,