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rs780233639

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs780233639(A;A)
Make rs780233639(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome5
Position126552106
GeneALDH7A1
is asnp
is mentioned by
dbSNPrs780233639
dbSNP (classic)rs780233639
ClinGenrs780233639
ebirs780233639
HLIrs780233639
Exacrs780233639
Gnomadrs780233639
Varsomers780233639
LitVarrs780233639
Maprs780233639
PheGenIrs780233639
Biobankrs780233639
1000 genomesrs780233639
hgdprs780233639
ensemblrs780233639
geneviewrs780233639
scholarrs780233639
googlers780233639
pharmgkbrs780233639
gwascentralrs780233639
openSNPrs780233639
23andMers780233639
SNPshotrs780233639
SNPdbers780233639
MSV3drs780233639
GWAS Ctlgrs780233639
Max Magnitude0
ClinVar
Risk rs780233639(A;A)
Alt rs780233639(A;A)
Reference Rs780233639(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene ALDH7A1
CLNDBN not provided
Reversed 0
HGVS NC_000005.9:g.125887798G>A
CLNSRC
CLNACC RCV000494142.1,