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rs587777605

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587777605(A;A)
Make rs587777605(A;G)
ReferenceGRCh38 38.1/142
ChromosomeX
Position107905593
GeneMID2, RP6-191P20.4
is asnp
is mentioned by
dbSNPrs587777605
ebirs587777605
HLIrs587777605
Exacrs587777605
Varsomers587777605
Maprs587777605
PheGenIrs587777605
hapmaprs587777605
1000 genomesrs587777605
hgdprs587777605
ensemblrs587777605
gopubmedrs587777605
geneviewrs587777605
scholarrs587777605
googlers587777605
pharmgkbrs587777605
gwascentralrs587777605
openSNPrs587777605
23andMers587777605
23andMe allrs587777605
SNP Nexus

SNPshotrs587777605
SNPdbers587777605
MSV3drs587777605
GWAS Ctlgrs587777605
Max Magnitude0
ClinVar
Risk rs587777605(A;A)
Alt rs587777605(A;A)
Reference rs587777605(G;G)
Significance Pathogenic
Disease Mental retardation
Variation info
Gene MID2 LOC101928335
CLNDBN Mental retardation, X-linked 101
Reversed 0
HGVS NC_000023.10:g.107148823G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000133396.3,