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rs886041708

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Chromosome14
Position54902505
GeneGCH1
is asnp
is mentioned by
dbSNPrs886041708
dbSNP (classic)rs886041708
ClinGenrs886041708
ebirs886041708
HLIrs886041708
Exacrs886041708
Gnomadrs886041708
Varsomers886041708
LitVarrs886041708
Maprs886041708
PheGenIrs886041708
Biobankrs886041708
1000 genomesrs886041708
hgdprs886041708
ensemblrs886041708
geneviewrs886041708
scholarrs886041708
googlers886041708
pharmgkbrs886041708
gwascentralrs886041708
openSNPrs886041708
23andMers886041708
23andMe allrs886041708
SNPshotrs886041708
SNPdbers886041708
MSV3drs886041708
GWAS Ctlgrs886041708
Max Magnitude0
ClinVar
Risk rs886041708(A;A)
Alt rs886041708(A;A)
Reference Rs886041708(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene GCH1
CLNDBN not provided
Reversed 1
HGVS NC_000014.8:g.55369223C>T
CLNSRC
CLNACC RCV000334247.1,