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rs724466

From SNPedia

Orientationminus
Stabilizedminus
Make rs724466(C;C)
Make rs724466(C;T)
Make rs724466(T;T)
ReferenceGRCh38 38.1/141
Chromosome16
Position22786531
is asnp
is mentioned by
dbSNPrs724466
dbSNP (classic)rs724466
ClinGenrs724466
ebirs724466
HLIrs724466
Exacrs724466
Gnomadrs724466
Varsomers724466
LitVarrs724466
Maprs724466
PheGenIrs724466
Biobankrs724466
1000 genomesrs724466
hgdprs724466
ensemblrs724466
geneviewrs724466
scholarrs724466
googlers724466
pharmgkbrs724466
gwascentralrs724466
openSNPrs724466
23andMers724466
23andMe allrs724466
SNPshotrs724466
SNPdbers724466
MSV3drs724466
GWAS Ctlgrs724466
GMAF0.2847
Max Magnitude0
? (C;C) (C;T) (T;T) 28


OMIM611096
DescMENTAL RETARDATION, AUTOSOMAL RECESSIVE 10; MRT10
Variant
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