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rs199497486

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs199497486(C;T)
Make rs199497486(T;T)
ReferenceGRCh38.p7 38.3/149
Chromosome5
Position126592663
GeneALDH7A1
is asnp
is mentioned by
dbSNPrs199497486
dbSNP (old)rs199497486
ClinGenrs199497486
ebirs199497486
HLIrs199497486
Exacrs199497486
Gnomadrs199497486
Varsomers199497486
LitVarrs199497486
Maprs199497486
PheGenIrs199497486
Biobankrs199497486
1000 genomesrs199497486
hgdprs199497486
ensemblrs199497486
gopubmedrs199497486
geneviewrs199497486
scholarrs199497486
googlers199497486
pharmgkbrs199497486
gwascentralrs199497486
openSNPrs199497486
23andMers199497486
23andMe allrs199497486
SNPshotrs199497486
SNPdbers199497486
MSV3drs199497486
GWAS Ctlgrs199497486
Max Magnitude0
ClinVar
Risk rs199497486(T;T)
Alt rs199497486(T;T)
Reference Rs199497486(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene ALDH7A1
CLNDBN not provided
Reversed 0
HGVS NC_000005.9:g.125928355C>T
CLNSRC
CLNACC RCV000255069.1,