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rs869312693

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs869312693(C;T)
Make rs869312693(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome14
Position102034135
GeneDYNC1H1
is asnp
is mentioned by
dbSNPrs869312693
ebirs869312693
HLIrs869312693
Exacrs869312693
Varsomers869312693
Maprs869312693
PheGenIrs869312693
hapmaprs869312693
1000 genomesrs869312693
hgdprs869312693
ensemblrs869312693
gopubmedrs869312693
geneviewrs869312693
scholarrs869312693
googlers869312693
pharmgkbrs869312693
gwascentralrs869312693
openSNPrs869312693
23andMers869312693
23andMe allrs869312693
SNP Nexus

SNPshotrs869312693
SNPdbers869312693
MSV3drs869312693
GWAS Ctlgrs869312693
Max Magnitude0
ClinVar
Risk rs869312693(T;T)
Alt rs869312693(T;T)
Reference rs869312693(C;C)
Significance Pathogenic
Disease Mental retardation
Variation info
Gene DYNC1H1
CLNDBN Mental retardation, autosomal dominant 13
Reversed 0
HGVS NC_000014.8:g.102500472C>T
CLNSRC
CLNACC RCV000209943.1,