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rs1780316

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1780316(C;C)
Make rs1780316(C;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position21563142
GeneALPL
is asnp
is mentioned by
dbSNPrs1780316
ebirs1780316
HLIrs1780316
Exacrs1780316
Varsomers1780316
Maprs1780316
PheGenIrs1780316
hapmaprs1780316
1000 genomesrs1780316
hgdprs1780316
ensemblrs1780316
gopubmedrs1780316
geneviewrs1780316
scholarrs1780316
googlers1780316
pharmgkbrs1780316
gwascentralrs1780316
openSNPrs1780316
23andMers1780316
23andMe allrs1780316
SNP Nexus

SNPshotrs1780316
SNPdbers1780316
MSV3drs1780316
GWAS Ctlgrs1780316
Max Magnitude0
? (C;C) (C;T) (T;T) 28
[PMID 25147783OA-icon.png] Genetic Associations with Plasma B12, B6, and Folate Levels in an Ischemic Stroke Population from the Vitamin Intervention for Stroke Prevention (VISP) Trial


ClinVar
Risk rs1780316(C;C)
Alt rs1780316(C;C)
Reference rs1780316(T;T)
Significance Non-pathogenic
Disease not specified
Variation info
Gene ALPL
CLNDBN not specified
Reversed 0
HGVS NC_000001.10:g.21889635T>C
CLNSRC
CLNACC RCV000178778.1,