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rs606231459

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs606231459(A;A)
Make rs606231459(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome5
Position150541651
GeneNDST1
is asnp
is mentioned by
dbSNPrs606231459
ebirs606231459
HLIrs606231459
Exacrs606231459
Varsomers606231459
Maprs606231459
PheGenIrs606231459
hapmaprs606231459
1000 genomesrs606231459
hgdprs606231459
ensemblrs606231459
gopubmedrs606231459
geneviewrs606231459
scholarrs606231459
googlers606231459
pharmgkbrs606231459
gwascentralrs606231459
openSNPrs606231459
23andMers606231459
23andMe allrs606231459
SNP Nexus

SNPshotrs606231459
SNPdbers606231459
MSV3drs606231459
GWAS Ctlgrs606231459
Max Magnitude0
ClinVar
Risk rs606231459(A;A)
Alt rs606231459(A;A)
Reference rs606231459(G;G)
Significance Pathogenic
Disease Mental retardation
Variation info
Gene NDST1
CLNDBN Mental retardation, autosomal recessive 46
Reversed 0
HGVS NC_000005.9:g.149921213G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000148928.4,