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rs121907932

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121907932(A;A)
Make rs121907932(A;G)
ReferenceGRCh38 38.1/142
Chromosome22
Position49910466
GeneALG12
is asnp
is mentioned by
dbSNPrs121907932
ebirs121907932
HLIrs121907932
Exacrs121907932
Varsomers121907932
Maprs121907932
PheGenIrs121907932
hapmaprs121907932
1000 genomesrs121907932
hgdprs121907932
ensemblrs121907932
gopubmedrs121907932
geneviewrs121907932
scholarrs121907932
googlers121907932
pharmgkbrs121907932
gwascentralrs121907932
openSNPrs121907932
23andMers121907932
23andMe allrs121907932
SNP Nexus

SNPshotrs121907932
SNPdbers121907932
MSV3drs121907932
GWAS Ctlgrs121907932
Max Magnitude0
OMIM607144
Desc
Variant0003
Relatedalso
ClinVar
Risk rs121907932(A;A)
Alt rs121907932(A;A)
Reference rs121907932(G;G)
Significance Pathogenic
Disease Congenital disorder of glycosylation type 1G
Variation info
Gene ALG12
CLNDBN Congenital disorder of glycosylation type 1G
Reversed 1
HGVS NC_000022.10:g.50304114C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000003604.3,