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rs869312864

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs869312864(C;T)
Make rs869312864(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome10
Position68487193
GeneSLC25A16
is asnp
is mentioned by
dbSNPrs869312864
ebirs869312864
HLIrs869312864
Exacrs869312864
Varsomers869312864
Maprs869312864
PheGenIrs869312864
hapmaprs869312864
1000 genomesrs869312864
hgdprs869312864
ensemblrs869312864
gopubmedrs869312864
geneviewrs869312864
scholarrs869312864
googlers869312864
pharmgkbrs869312864
gwascentralrs869312864
openSNPrs869312864
23andMers869312864
23andMe allrs869312864
SNP Nexus

SNPshotrs869312864
SNPdbers869312864
MSV3drs869312864
GWAS Ctlgrs869312864
Max Magnitude0
ClinVar
Risk rs869312864(T;T)
Alt rs869312864(T;T)
Reference rs869312864(C;C)
Significance Probable-Pathogenic
Disease Cerebral visual impairment and intellectual disability
Variation info
Gene SLC25A16
CLNDBN Cerebral visual impairment and intellectual disability
Reversed 1
HGVS NC_000010.10:g.70246950G>A
CLNSRC
CLNACC RCV000210396.1,