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rs376917645

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs376917645(A;A)
Make rs376917645(A;G)
ReferenceGRCh38.p7 38.3/149
Chromosome5
Position126577154
GeneALDH7A1
is asnp
is mentioned by
dbSNPrs376917645
dbSNP (classic)rs376917645
ClinGenrs376917645
ebirs376917645
HLIrs376917645
Exacrs376917645
Gnomadrs376917645
Varsomers376917645
LitVarrs376917645
Maprs376917645
PheGenIrs376917645
Biobankrs376917645
1000 genomesrs376917645
hgdprs376917645
ensemblrs376917645
geneviewrs376917645
scholarrs376917645
googlers376917645
pharmgkbrs376917645
gwascentralrs376917645
openSNPrs376917645
23andMers376917645
SNPshotrs376917645
SNPdbers376917645
MSV3drs376917645
GWAS Ctlgrs376917645
Max Magnitude0
ClinVar
Risk rs376917645(A;A)
Alt rs376917645(A;A)
Reference Rs376917645(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene ALDH7A1
CLNDBN not provided
Reversed 0
HGVS NC_000005.9:g.125912846G>A
CLNSRC
CLNACC RCV000255618.1,