Have questions? Visit https://www.reddit.com/r/SNPedia

rs587776908

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587776908(C;T)
Make rs587776908(T;T)
ReferenceGRCh38 38.1/142
Chromosome5
Position6600195
GeneNSUN2
is asnp
is mentioned by
dbSNPrs587776908
ebirs587776908
HLIrs587776908
Exacrs587776908
Varsomers587776908
Maprs587776908
PheGenIrs587776908
hapmaprs587776908
1000 genomesrs587776908
hgdprs587776908
ensemblrs587776908
gopubmedrs587776908
geneviewrs587776908
scholarrs587776908
googlers587776908
pharmgkbrs587776908
gwascentralrs587776908
openSNPrs587776908
23andMers587776908
23andMe allrs587776908
SNP Nexus

SNPshotrs587776908
SNPdbers587776908
MSV3drs587776908
GWAS Ctlgrs587776908
Max Magnitude0
ClinVar
Risk rs587776908(T;T)
Alt rs587776908(T;T)
Reference rs587776908(C;C)
Significance Pathogenic
Disease Mental retardation
Variation info
Gene NSUN2
CLNDBN Mental retardation, autosomal recessive 5
Reversed 0
HGVS NC_000005.9:g.6600308C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000024358.2,