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rs398122869

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(CT;CT) 0 common in clinvar
(TC;TC) 0 common in clinvar
Make rs398122869(-;-)
Make rs398122869(-;TC)
ReferenceGRCh38 38.1/141
Chromosome19
Position13078668
GeneNFIX
is asnp
is mentioned by
dbSNPrs398122869
ebirs398122869
HLIrs398122869
Exacrs398122869
Varsomers398122869
Maprs398122869
PheGenIrs398122869
hapmaprs398122869
1000 genomesrs398122869
hgdprs398122869
ensemblrs398122869
gopubmedrs398122869
geneviewrs398122869
scholarrs398122869
googlers398122869
pharmgkbrs398122869
gwascentralrs398122869
openSNPrs398122869
23andMers398122869
23andMe allrs398122869
SNP Nexus

SNPshotrs398122869
SNPdbers398122869
MSV3drs398122869
GWAS Ctlgrs398122869
Max Magnitude0
ClinVar
Risk rs398122869(;)
Alt rs398122869(;)
Reference rs398122869(CT;CT)
Significance Pathogenic
Disease Marshall-Smith syndrome
Variation info
Gene NFIX
CLNDBN Marshall-Smith syndrome
Reversed 0
HGVS NC_000019.9:g.13189482_13189483delTC
CLNSRC OMIM Allelic Variant
CLNACC RCV000030637.21,