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rs587777161

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587777161(A;A)
Make rs587777161(A;G)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position10213734
GeneCLCN4
is asnp
is mentioned by
dbSNPrs587777161
ebirs587777161
HLIrs587777161
Exacrs587777161
Varsomers587777161
Maprs587777161
PheGenIrs587777161
hapmaprs587777161
1000 genomesrs587777161
hgdprs587777161
ensemblrs587777161
gopubmedrs587777161
geneviewrs587777161
scholarrs587777161
googlers587777161
pharmgkbrs587777161
gwascentralrs587777161
openSNPrs587777161
23andMers587777161
23andMe allrs587777161
SNP Nexus

SNPshotrs587777161
SNPdbers587777161
MSV3drs587777161
GWAS Ctlgrs587777161
Max Magnitude0
ClinVar
Risk rs587777161(A;A)
Alt rs587777161(A;A)
Reference rs587777161(G;G)
Significance Pathogenic
Disease Mental retardation 49
Variation info
Gene CLCN4
CLNDBN Mental retardation 49, X-linked
Reversed 0
HGVS NC_000023.10:g.10181774G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000087143.4,