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rs119103238

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs119103238(A;A)
Make rs119103238(A;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position184245333
GeneALG3
is asnp
is mentioned by
dbSNPrs119103238
ebirs119103238
HLIrs119103238
Exacrs119103238
Varsomers119103238
Maprs119103238
PheGenIrs119103238
hapmaprs119103238
1000 genomesrs119103238
hgdprs119103238
ensemblrs119103238
gopubmedrs119103238
geneviewrs119103238
scholarrs119103238
googlers119103238
pharmgkbrs119103238
gwascentralrs119103238
openSNPrs119103238
23andMers119103238
23andMe allrs119103238
SNP Nexus

SNPshotrs119103238
SNPdbers119103238
MSV3drs119103238
GWAS Ctlgrs119103238
Max Magnitude0
OMIM608750
Desc
Variant0005
Relatedalso
ClinVar
Risk rs119103238(A,C;A,C)
Alt rs119103238(A,C;A,C)
Reference rs119103238(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.183963121A>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000002213.3,