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rs121912597

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common on affy axiom data
Make rs121912597(C;T)
Make rs121912597(T;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position143493701
GeneSLC9A9
is asnp
is mentioned by
dbSNPrs121912597
ebirs121912597
HLIrs121912597
Exacrs121912597
Varsomers121912597
Maprs121912597
PheGenIrs121912597
hapmaprs121912597
1000 genomesrs121912597
hgdprs121912597
ensemblrs121912597
gopubmedrs121912597
geneviewrs121912597
scholarrs121912597
googlers121912597
pharmgkbrs121912597
gwascentralrs121912597
openSNPrs121912597
23andMers121912597
23andMe allrs121912597
SNP Nexus

SNPshotrs121912597
SNPdbers121912597
MSV3drs121912597
GWAS Ctlgrs121912597
GMAF0.0004591
Max Magnitude0
OMIM608396
Desc
Variant0001
Relatedalso
ClinVar
Risk rs121912597(T;T)
Alt rs121912597(T;T)
Reference rs121912597(C;C)
Significance Other
Disease Autism 16
Variation info
Gene SLC9A9
CLNDBN Autism 16
Reversed 1
HGVS NC_000003.11:g.143212543G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000002459.3,