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rs1105434

From SNPedia

Orientationplus
Stabilizedplus
Make rs1105434(A;A)
Make rs1105434(A;G)
Make rs1105434(G;G)
ReferenceGRCh38 38.1/141
Chromosome4
Position56927585
GeneREST
is asnp
is mentioned by
dbSNPrs1105434
ebirs1105434
HLIrs1105434
Exacrs1105434
Varsomers1105434
Maprs1105434
PheGenIrs1105434
hapmaprs1105434
1000 genomesrs1105434
hgdprs1105434
ensemblrs1105434
gopubmedrs1105434
geneviewrs1105434
scholarrs1105434
googlers1105434
pharmgkbrs1105434
gwascentralrs1105434
openSNPrs1105434
23andMers1105434
23andMe allrs1105434
SNP Nexus

SNPshotrs1105434
SNPdbers1105434
MSV3drs1105434
GWAS Ctlgrs1105434
GMAF0.3122
Max Magnitude
? (A;A) (A;G) (G;G) 28
OMIM612713
DescKAHRIZI SYNDROME
Variant
Relatedalso
[PMID 18781183OA-icon.png] An autosomal recessive syndrome of severe mental retardation, cataract, coloboma and kyphosis maps to the pericentromeric region of chromosome 4.