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rs761221480

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs761221480(-;-)
Make rs761221480(-;C)
ReferenceGRCh38.p2 38.2/147
Chromosome22
Position49913649
GeneALG12
is asnp
is mentioned by
dbSNPrs761221480
ebirs761221480
HLIrs761221480
Exacrs761221480
Varsomers761221480
Maprs761221480
PheGenIrs761221480
hapmaprs761221480
1000 genomesrs761221480
hgdprs761221480
ensemblrs761221480
gopubmedrs761221480
geneviewrs761221480
scholarrs761221480
googlers761221480
pharmgkbrs761221480
gwascentralrs761221480
openSNPrs761221480
23andMers761221480
23andMe allrs761221480
SNP Nexus

SNPshotrs761221480
SNPdbers761221480
MSV3drs761221480
GWAS Ctlgrs761221480
Max Magnitude0
ClinVar
Risk rs761221480(;)
Alt rs761221480(;)
Reference rs761221480(C;C)
Significance Pathogenic
Disease Congenital disorder of glycosylation type 1G
Variation info
Gene ALG12
CLNDBN Congenital disorder of glycosylation type 1G
Reversed 0
HGVS NC_000022.10:g.50307297delC
CLNSRC
CLNACC RCV000234907.1,