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rs556400964

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs556400964(C;G)
Make rs556400964(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome5
Position126546376
GeneALDH7A1
is asnp
is mentioned by
dbSNPrs556400964
ebirs556400964
HLIrs556400964
Exacrs556400964
Varsomers556400964
Maprs556400964
PheGenIrs556400964
hapmaprs556400964
1000 genomesrs556400964
hgdprs556400964
ensemblrs556400964
gopubmedrs556400964
geneviewrs556400964
scholarrs556400964
googlers556400964
pharmgkbrs556400964
gwascentralrs556400964
openSNPrs556400964
23andMers556400964
23andMe allrs556400964
SNP Nexus

SNPshotrs556400964
SNPdbers556400964
MSV3drs556400964
GWAS Ctlgrs556400964
Max Magnitude0
ClinVar
Risk rs556400964(G;G)
Alt rs556400964(G;G)
Reference rs556400964(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene ALDH7A1
CLNDBN not provided
Reversed 0
HGVS NC_000005.9:g.125882068C>G
CLNSRC
CLNACC RCV000186750.2,