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rs398124645

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs398124645(A;G)
Make rs398124645(G;G)
ReferenceGRCh38 38.1/141
Chromosome8
Position119783548
GeneTAF2
is asnp
is mentioned by
dbSNPrs398124645
ebirs398124645
HLIrs398124645
Exacrs398124645
Varsomers398124645
Maprs398124645
PheGenIrs398124645
hapmaprs398124645
1000 genomesrs398124645
hgdprs398124645
ensemblrs398124645
gopubmedrs398124645
geneviewrs398124645
scholarrs398124645
googlers398124645
pharmgkbrs398124645
gwascentralrs398124645
openSNPrs398124645
23andMers398124645
23andMe allrs398124645
SNP Nexus

SNPshotrs398124645
SNPdbers398124645
MSV3drs398124645
GWAS Ctlgrs398124645
Max Magnitude0
ClinVar
Risk rs398124645(G;G)
Alt rs398124645(G;G)
Reference rs398124645(A;A)
Significance Pathogenic
Disease Mental retardation
Variation info
Gene TAF2
CLNDBN Mental retardation, autosomal recessive 40
Reversed 0
HGVS NC_000008.10:g.120795788A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000077872.2,