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rs201948406

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs201948406(C;T)
Make rs201948406(T;T)
ReferenceGRCh38.p7 38.3/149
Chromosome5
Position126568296
GeneALDH7A1
is asnp
is mentioned by
dbSNPrs201948406
dbSNP (old)rs201948406
ClinGenrs201948406
ebirs201948406
HLIrs201948406
Exacrs201948406
Gnomadrs201948406
Varsomers201948406
LitVarrs201948406
Maprs201948406
PheGenIrs201948406
Biobankrs201948406
1000 genomesrs201948406
hgdprs201948406
ensemblrs201948406
gopubmedrs201948406
geneviewrs201948406
scholarrs201948406
googlers201948406
pharmgkbrs201948406
gwascentralrs201948406
openSNPrs201948406
23andMers201948406
23andMe allrs201948406
SNPshotrs201948406
SNPdbers201948406
MSV3drs201948406
GWAS Ctlgrs201948406
Max Magnitude0
ClinVar
Risk rs201948406(A;A) rs201948406(G;G) rs201948406(T;T)
Alt rs201948406(A;A) rs201948406(G;G) rs201948406(T;T)
Reference Rs201948406(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene ALDH7A1
CLNDBN not provided
Reversed 0
HGVS NC_000005.9:g.125903988C>T
CLNSRC
CLNACC RCV000255917.2,