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rs747597620

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs747597620(C;C)
Make rs747597620(C;T)
ReferenceGRCh38.p2 38.2/144
Chromosome5
Position126552037
GeneALDH7A1
is asnp
is mentioned by
dbSNPrs747597620
ebirs747597620
HLIrs747597620
Exacrs747597620
Varsomers747597620
Maprs747597620
PheGenIrs747597620
hapmaprs747597620
1000 genomesrs747597620
hgdprs747597620
ensemblrs747597620
gopubmedrs747597620
geneviewrs747597620
scholarrs747597620
googlers747597620
pharmgkbrs747597620
gwascentralrs747597620
openSNPrs747597620
23andMers747597620
23andMe allrs747597620
SNP Nexus

SNPshotrs747597620
SNPdbers747597620
MSV3drs747597620
GWAS Ctlgrs747597620
Max Magnitude0
ClinVar
Risk rs747597620(C;C)
Alt rs747597620(C;C)
Reference rs747597620(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene ALDH7A1
CLNDBN not provided
Reversed 0
HGVS NC_000005.9:g.125887729T>C
CLNSRC
CLNACC RCV000186746.1,