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rs869312858

From SNPedia

Orientationminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs869312858(-;-)
Make rs869312858(-;T)
Make rs869312858(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome1
Position27550713
GeneAHDC1
is asnp
is mentioned by
dbSNPrs869312858
ebirs869312858
HLIrs869312858
Exacrs869312858
Varsomers869312858
Maprs869312858
PheGenIrs869312858
hapmaprs869312858
1000 genomesrs869312858
hgdprs869312858
ensemblrs869312858
gopubmedrs869312858
geneviewrs869312858
scholarrs869312858
googlers869312858
pharmgkbrs869312858
gwascentralrs869312858
openSNPrs869312858
23andMers869312858
23andMe allrs869312858
SNP Nexus

SNPshotrs869312858
SNPdbers869312858
MSV3drs869312858
GWAS Ctlgrs869312858
Max Magnitude0
ClinVar
Risk rs869312858(T;T)
Alt rs869312858(T;T)
Reference rs869312858(;)
Significance Pathogenic
Disease Cerebral visual impairment and intellectual disability
Variation info
Gene AHDC1
CLNDBN Cerebral visual impairment and intellectual disability
Reversed 1
HGVS NC_000001.10:g.27877225dupA
CLNSRC
CLNACC RCV000210395.1,