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rs1057524499

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1057524499(A;T)
Make rs1057524499(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome19
Position1399005
GeneGAMT
is asnp
is mentioned by
dbSNPrs1057524499
dbSNP (old)rs1057524499
ClinGenrs1057524499
ebirs1057524499
HLIrs1057524499
Exacrs1057524499
Gnomadrs1057524499
Varsomers1057524499
Maprs1057524499
PheGenIrs1057524499
Biobankrs1057524499
1000 genomesrs1057524499
hgdprs1057524499
ensemblrs1057524499
gopubmedrs1057524499
geneviewrs1057524499
scholarrs1057524499
googlers1057524499
pharmgkbrs1057524499
gwascentralrs1057524499
openSNPrs1057524499
23andMers1057524499
23andMe allrs1057524499
SNPshotrs1057524499
SNPdbers1057524499
MSV3drs1057524499
GWAS Ctlgrs1057524499
Max Magnitude0
ClinVar
Risk rs1057524499(T;T)
Alt rs1057524499(T;T)
Reference Rs1057524499(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene GAMT
CLNDBN not provided
Reversed 1
HGVS NC_000019.9:g.1399004T>A
CLNSRC
CLNACC RCV000420204.1,