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rs754449549

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs754449549(C;T)
Make rs754449549(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome5
Position126559244
GeneALDH7A1
is asnp
is mentioned by
dbSNPrs754449549
ebirs754449549
HLIrs754449549
Exacrs754449549
Varsomers754449549
Maprs754449549
PheGenIrs754449549
hapmaprs754449549
1000 genomesrs754449549
hgdprs754449549
ensemblrs754449549
gopubmedrs754449549
geneviewrs754449549
scholarrs754449549
googlers754449549
pharmgkbrs754449549
gwascentralrs754449549
openSNPrs754449549
23andMers754449549
23andMe allrs754449549
SNP Nexus

SNPshotrs754449549
SNPdbers754449549
MSV3drs754449549
GWAS Ctlgrs754449549
Max Magnitude0
ClinVar
Risk rs754449549(T;T)
Alt rs754449549(T;T)
Reference rs754449549(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene ALDH7A1
CLNDBN not provided
Reversed 0
HGVS NC_000005.9:g.125894936C>T
CLNSRC
CLNACC RCV000186728.2,