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rs398122872

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs398122872(-;-)
Make rs398122872(-;C)
Make rs398122872(C;C)
ReferenceGRCh38 38.1/141
Chromosome19
Position13078705
GeneNFIX
is asnp
is mentioned by
dbSNPrs398122872
ebirs398122872
HLIrs398122872
Exacrs398122872
Varsomers398122872
Maprs398122872
PheGenIrs398122872
hapmaprs398122872
1000 genomesrs398122872
hgdprs398122872
ensemblrs398122872
gopubmedrs398122872
geneviewrs398122872
scholarrs398122872
googlers398122872
pharmgkbrs398122872
gwascentralrs398122872
openSNPrs398122872
23andMers398122872
23andMe allrs398122872
SNP Nexus

SNPshotrs398122872
SNPdbers398122872
MSV3drs398122872
GWAS Ctlgrs398122872
Max Magnitude0
ClinVar
Risk rs398122872(C;C)
Alt rs398122872(C;C)
Reference rs398122872(;)
Significance Pathogenic
Disease Marshall-Smith syndrome
Variation info
Gene NFIX
CLNDBN Marshall-Smith syndrome
Reversed 0
HGVS NC_000019.9:g.13189520dupC
CLNSRC OMIM Allelic Variant
CLNACC RCV000030640.25,