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rs1599711

From SNPedia

Orientationminus
Stabilizedminus
Make rs1599711(C;C)
Make rs1599711(C;T)
Make rs1599711(T;T)
ReferenceGRCh38 38.1/142
Chromosome10
Position69611373
is asnp
is mentioned by
dbSNPrs1599711
dbSNP (classic)rs1599711
ClinGenrs1599711
ebirs1599711
HLIrs1599711
Exacrs1599711
Gnomadrs1599711
Varsomers1599711
LitVarrs1599711
Maprs1599711
PheGenIrs1599711
Biobankrs1599711
1000 genomesrs1599711
hgdprs1599711
ensemblrs1599711
geneviewrs1599711
scholarrs1599711
googlers1599711
pharmgkbrs1599711
gwascentralrs1599711
openSNPrs1599711
23andMers1599711
23andMe allrs1599711
SNPshotrs1599711
SNPdbers1599711
MSV3drs1599711
GWAS Ctlgrs1599711
GMAF0.2539
Max Magnitude0
? (C;C) (C;T) (T;T) 28


OMIM611094
DescMENTAL RETARDATION, AUTOSOMAL RECESSIVE 8; MRT8
Variant
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