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rs121907935

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121907935(C;G)
Make rs121907935(G;G)
ReferenceGRCh38 38.1/141
Chromosome22
Position49904063
GeneALG12
is asnp
is mentioned by
dbSNPrs121907935
ebirs121907935
HLIrs121907935
Exacrs121907935
Varsomers121907935
Maprs121907935
PheGenIrs121907935
hapmaprs121907935
1000 genomesrs121907935
hgdprs121907935
ensemblrs121907935
gopubmedrs121907935
geneviewrs121907935
scholarrs121907935
googlers121907935
pharmgkbrs121907935
gwascentralrs121907935
openSNPrs121907935
23andMers121907935
23andMe allrs121907935
SNP Nexus

SNPshotrs121907935
SNPdbers121907935
MSV3drs121907935
GWAS Ctlgrs121907935
Max Magnitude0
OMIM607144
Desc
Variant0006
Relatedalso
ClinVar
Risk rs121907935(G,T;G,T)
Alt rs121907935(G,T;G,T)
Reference rs121907935(C;C)
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.50297711G>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000003607.3,