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rs398122874

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs398122874(-;-)
Make rs398122874(-;T)
Make rs398122874(T;T)
ReferenceGRCh38 38.1/141
Chromosome19
Position13078651
GeneNFIX
is asnp
is mentioned by
dbSNPrs398122874
ebirs398122874
HLIrs398122874
Exacrs398122874
Varsomers398122874
Maprs398122874
PheGenIrs398122874
hapmaprs398122874
1000 genomesrs398122874
hgdprs398122874
ensemblrs398122874
gopubmedrs398122874
geneviewrs398122874
scholarrs398122874
googlers398122874
pharmgkbrs398122874
gwascentralrs398122874
openSNPrs398122874
23andMers398122874
23andMe allrs398122874
SNP Nexus

SNPshotrs398122874
SNPdbers398122874
MSV3drs398122874
GWAS Ctlgrs398122874
Max Magnitude0
ClinVar
Risk rs398122874(T;T)
Alt rs398122874(T;T)
Reference rs398122874(;)
Significance Pathogenic
Disease Marshall-Smith syndrome
Variation info
Gene NFIX
CLNDBN Marshall-Smith syndrome
Reversed 0
HGVS NC_000019.9:g.13189465dupT
CLNSRC OMIM Allelic Variant
CLNACC RCV000030642.25,