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

rs869312866

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs869312866(A;A)
Make rs869312866(A;C)
ReferenceGRCh38.p2 38.2/147
Chromosome16
Position67320674
GeneKCTD19
is asnp
is mentioned by
dbSNPrs869312866
ebirs869312866
HLIrs869312866
Exacrs869312866
Varsomers869312866
Maprs869312866
PheGenIrs869312866
hapmaprs869312866
1000 genomesrs869312866
hgdprs869312866
ensemblrs869312866
gopubmedrs869312866
geneviewrs869312866
scholarrs869312866
googlers869312866
pharmgkbrs869312866
gwascentralrs869312866
openSNPrs869312866
23andMers869312866
23andMe allrs869312866
SNP Nexus

SNPshotrs869312866
SNPdbers869312866
MSV3drs869312866
GWAS Ctlgrs869312866
Max Magnitude0
ClinVar
Risk rs869312866(A;A)
Alt rs869312866(A;A)
Reference rs869312866(C;C)
Significance Probable-Pathogenic
Disease Cerebral visual impairment and intellectual disability
Variation info
Gene KCTD19
CLNDBN Cerebral visual impairment and intellectual disability
Reversed 1
HGVS NC_000016.9:g.67354577G>T
CLNSRC
CLNACC RCV000210400.1,