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rs752922461

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs752922461(C;T)
Make rs752922461(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome16
Position5071864
GeneALG1
is asnp
is mentioned by
dbSNPrs752922461
ebirs752922461
HLIrs752922461
Exacrs752922461
Varsomers752922461
Maprs752922461
PheGenIrs752922461
hapmaprs752922461
1000 genomesrs752922461
hgdprs752922461
ensemblrs752922461
gopubmedrs752922461
geneviewrs752922461
scholarrs752922461
googlers752922461
pharmgkbrs752922461
gwascentralrs752922461
openSNPrs752922461
23andMers752922461
23andMe allrs752922461
SNP Nexus

SNPshotrs752922461
SNPdbers752922461
MSV3drs752922461
GWAS Ctlgrs752922461
Max Magnitude0
ClinVar
Risk rs752922461(A,T;A,T)
Alt rs752922461(A,T;A,T)
Reference rs752922461(C;C)
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.5121865C>A
CLNSRC
CLNACC RCV000173489.1,