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rs555896752

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs555896752(A;C)
Make rs555896752(C;C)
ReferenceGRCh38.p2 38.2/144
Chromosome5
Position126577122
GeneALDH7A1
is asnp
is mentioned by
dbSNPrs555896752
ebirs555896752
HLIrs555896752
Exacrs555896752
Varsomers555896752
Maprs555896752
PheGenIrs555896752
hapmaprs555896752
1000 genomesrs555896752
hgdprs555896752
ensemblrs555896752
gopubmedrs555896752
geneviewrs555896752
scholarrs555896752
googlers555896752
pharmgkbrs555896752
gwascentralrs555896752
openSNPrs555896752
23andMers555896752
23andMe allrs555896752
SNP Nexus

SNPshotrs555896752
SNPdbers555896752
MSV3drs555896752
GWAS Ctlgrs555896752
Max Magnitude0
ClinVar
Risk rs555896752(C;C)
Alt rs555896752(C;C)
Reference rs555896752(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene ALDH7A1
CLNDBN not provided
Reversed 0
HGVS NC_000005.9:g.125912814A>C
CLNSRC
CLNACC RCV000186727.2,