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rs786205614

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs786205614(A;G)
Make rs786205614(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome10
Position95637408
GeneALDH18A1
is asnp
is mentioned by
dbSNPrs786205614
ebirs786205614
HLIrs786205614
Exacrs786205614
Varsomers786205614
Maprs786205614
PheGenIrs786205614
hapmaprs786205614
1000 genomesrs786205614
hgdprs786205614
ensemblrs786205614
gopubmedrs786205614
geneviewrs786205614
scholarrs786205614
googlers786205614
pharmgkbrs786205614
gwascentralrs786205614
openSNPrs786205614
23andMers786205614
23andMe allrs786205614
SNP Nexus

SNPshotrs786205614
SNPdbers786205614
MSV3drs786205614
GWAS Ctlgrs786205614
Max Magnitude0
ClinVar
Risk rs786205614(G;G)
Alt rs786205614(G;G)
Reference rs786205614(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene ALDH18A1
CLNDBN not provided
Reversed 1
HGVS NC_000010.10:g.97397165T>C
CLNSRC
CLNACC RCV000171459.1,