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rs1113990

From SNPedia

Orientationminus
Stabilizedminus
Make rs1113990(C;C)
Make rs1113990(C;G)
Make rs1113990(G;G)
ReferenceGRCh38 38.1/141
Chromosome8
Position28845282
GeneINTS9
is asnp
is mentioned by
dbSNPrs1113990
ebirs1113990
HLIrs1113990
Exacrs1113990
Varsomers1113990
Maprs1113990
PheGenIrs1113990
hapmaprs1113990
1000 genomesrs1113990
hgdprs1113990
ensemblrs1113990
gopubmedrs1113990
geneviewrs1113990
scholarrs1113990
googlers1113990
pharmgkbrs1113990
gwascentralrs1113990
openSNPrs1113990
23andMers1113990
23andMe allrs1113990
SNP Nexus

SNPshotrs1113990
SNPdbers1113990
MSV3drs1113990
GWAS Ctlgrs1113990
GMAF0.4545
Max Magnitude
? (C;C) (C;G) (G;G) 28
OMIM611093
DescMENTAL RETARDATION, AUTOSOMAL RECESSIVE 7; MRT7
Variant
Relatedalso