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rs374928784

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs374928784(A;A)
Make rs374928784(A;G)
ReferenceGRCh38 38.1/141
Chromosome16
Position5082674
GeneALG1
is asnp
is mentioned by
dbSNPrs374928784
ebirs374928784
HLIrs374928784
Exacrs374928784
Varsomers374928784
Maprs374928784
PheGenIrs374928784
hapmaprs374928784
1000 genomesrs374928784
hgdprs374928784
ensemblrs374928784
gopubmedrs374928784
geneviewrs374928784
scholarrs374928784
googlers374928784
pharmgkbrs374928784
gwascentralrs374928784
openSNPrs374928784
23andMers374928784
23andMe allrs374928784
SNP Nexus

SNPshotrs374928784
SNPdbers374928784
MSV3drs374928784
GWAS Ctlgrs374928784
Max Magnitude0
ClinVar
Risk rs374928784(A;A)
Alt rs374928784(A;A)
Reference rs374928784(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene ALG1
CLNDBN not provided
Reversed 0
HGVS NC_000016.9:g.5132675G>A
CLNSRC ClinVar
CLNACC RCV000081984.4,