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rs1064796560

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Chromosome14
Position54902363
GeneGCH1
is asnp
is mentioned by
dbSNPrs1064796560
dbSNP (old)rs1064796560
ClinGenrs1064796560
ebirs1064796560
HLIrs1064796560
Exacrs1064796560
Gnomadrs1064796560
Varsomers1064796560
Maprs1064796560
PheGenIrs1064796560
Biobankrs1064796560
1000 genomesrs1064796560
hgdprs1064796560
ensemblrs1064796560
gopubmedrs1064796560
geneviewrs1064796560
scholarrs1064796560
googlers1064796560
pharmgkbrs1064796560
gwascentralrs1064796560
openSNPrs1064796560
23andMers1064796560
23andMe allrs1064796560
SNPshotrs1064796560
SNPdbers1064796560
MSV3drs1064796560
GWAS Ctlgrs1064796560
Max Magnitude0
ClinVar
Risk rs1064796560(A;A)
Alt rs1064796560(A;A)
Reference Rs1064796560(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene GCH1
CLNDBN not provided
Reversed 1
HGVS NC_000014.8:g.55369081C>T
CLNSRC
CLNACC RCV000481039.1,