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rs149266909

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs149266909(A;T)
Make rs149266909(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome21
Position46137006
GeneFTCD
is asnp
is mentioned by
dbSNPrs149266909
ebirs149266909
HLIrs149266909
Exacrs149266909
Varsomers149266909
Maprs149266909
PheGenIrs149266909
hapmaprs149266909
1000 genomesrs149266909
hgdprs149266909
ensemblrs149266909
gopubmedrs149266909
geneviewrs149266909
scholarrs149266909
googlers149266909
pharmgkbrs149266909
gwascentralrs149266909
openSNPrs149266909
23andMers149266909
23andMe allrs149266909
SNP Nexus

SNPshotrs149266909
SNPdbers149266909
MSV3drs149266909
GWAS Ctlgrs149266909
Max Magnitude0
ClinVar
Risk rs149266909(T;T)
Alt rs149266909(T;T)
Reference rs149266909(A;A)
Significance Pathogenic
Disease GLUTAMATE FORMIMINOTRANSFERASE DEFICIENCY
Variation info
Gene FTCD
CLNDBN GLUTAMATE FORMIMINOTRANSFERASE DEFICIENCY
Reversed 0
HGVS NC_000021.8:g.47556920A>T
CLNSRC
CLNACC RCV000174758.1,