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rs796052267

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs796052267(-;-)
Make rs796052267(-;G)
ReferenceGRCh38.p2 38.2/146
Chromosome5
Position126549950
GeneALDH7A1
is asnp
is mentioned by
dbSNPrs796052267
ebirs796052267
HLIrs796052267
Exacrs796052267
Varsomers796052267
Maprs796052267
PheGenIrs796052267
hapmaprs796052267
1000 genomesrs796052267
hgdprs796052267
ensemblrs796052267
gopubmedrs796052267
geneviewrs796052267
scholarrs796052267
googlers796052267
pharmgkbrs796052267
gwascentralrs796052267
openSNPrs796052267
23andMers796052267
23andMe allrs796052267
SNP Nexus

SNPshotrs796052267
SNPdbers796052267
MSV3drs796052267
GWAS Ctlgrs796052267
Max Magnitude0
ClinVar
Risk rs796052267(;)
Alt rs796052267(;)
Reference rs796052267(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene ALDH7A1
CLNDBN not provided
Reversed 1
HGVS NC_000005.9:g.125885642delC
CLNSRC
CLNACC RCV000186757.1,