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

rs149908903

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs149908903(G;T)
Make rs149908903(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome1
Position17697186
GeneARHGEF10L
is asnp
is mentioned by
dbSNPrs149908903
ebirs149908903
HLIrs149908903
Exacrs149908903
Varsomers149908903
Maprs149908903
PheGenIrs149908903
hapmaprs149908903
1000 genomesrs149908903
hgdprs149908903
ensemblrs149908903
gopubmedrs149908903
geneviewrs149908903
scholarrs149908903
googlers149908903
pharmgkbrs149908903
gwascentralrs149908903
openSNPrs149908903
23andMers149908903
23andMe allrs149908903
SNP Nexus

SNPshotrs149908903
SNPdbers149908903
MSV3drs149908903
GWAS Ctlgrs149908903
Max Magnitude0
ClinVar
Risk rs149908903(T;T)
Alt rs149908903(T;T)
Reference rs149908903(G;G)
Significance Probable-Pathogenic
Disease Cerebral visual impairment and intellectual disability
Variation info
Gene ARHGEF10L
CLNDBN Cerebral visual impairment and intellectual disability
Reversed 0
HGVS NC_000001.10:g.18023681G>A
CLNSRC
CLNACC RCV000210382.1,