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rs267606651

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs267606651(A;C)
Make rs267606651(C;C)
ReferenceGRCh38 38.1/141
Chromosome16
Position5081009
GeneALG1
is asnp
is mentioned by
dbSNPrs267606651
ebirs267606651
HLIrs267606651
Exacrs267606651
Varsomers267606651
Maprs267606651
PheGenIrs267606651
hapmaprs267606651
1000 genomesrs267606651
hgdprs267606651
ensemblrs267606651
gopubmedrs267606651
geneviewrs267606651
scholarrs267606651
googlers267606651
pharmgkbrs267606651
gwascentralrs267606651
openSNPrs267606651
23andMers267606651
23andMe allrs267606651
SNP Nexus

SNPshotrs267606651
SNPdbers267606651
MSV3drs267606651
GWAS Ctlgrs267606651
Max Magnitude0
ClinVar
Risk rs267606651(C;C)
Alt rs267606651(C;C)
Reference rs267606651(A;A)
Significance Pathogenic
Disease Congenital disorder of glycosylation type 1K
Variation info
Gene ALG1
CLNDBN Congenital disorder of glycosylation type 1K
Reversed 0
HGVS NC_000016.9:g.5131010A>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000004990.5,