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rs55776826

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs55776826(C;T)
Make rs55776826(T;T)
ReferenceGRCh38 38.1/142
Chromosome19
Position1399057
GeneGAMT
is asnp
is mentioned by
dbSNPrs55776826
dbSNP (old)rs55776826
ClinGenrs55776826
ebirs55776826
HLIrs55776826
Exacrs55776826
Gnomadrs55776826
Varsomers55776826
Maprs55776826
PheGenIrs55776826
Biobankrs55776826
1000 genomesrs55776826
hgdprs55776826
ensemblrs55776826
gopubmedrs55776826
geneviewrs55776826
scholarrs55776826
googlers55776826
pharmgkbrs55776826
gwascentralrs55776826
openSNPrs55776826
23andMers55776826
23andMe allrs55776826
SNP Nexus

SNPshotrs55776826
SNPdbers55776826
MSV3drs55776826
GWAS Ctlgrs55776826
Max Magnitude0
rs55776826, also known as c.459+71G>A, is a SNP in the fourth intron of the guanidinoacetate N-methyltransferase GAMT gene on chromosome 19.

rs55776826 been reported as most likely to be a clinically benign polymorphism.[PMID 15108290]


ClinVar
Risk rs55776826(T;T)
Alt rs55776826(T;T)
Reference Rs55776826(C;C)
Significance Non-pathogenic
Disease Deficiency of guanidinoacetate methyltransferase
Variation info
Gene GAMT
CLNDBN Deficiency of guanidinoacetate methyltransferase
Reversed 0
HGVS NC_000019.9:g.1399056C>T
CLNSRC ClinVar GeneReviews
CLNACC RCV000020143.2,