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rs398122870

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs398122870(-;-)
Make rs398122870(-;T)
Make rs398122870(T;T)
ReferenceGRCh38 38.1/141
Chromosome19
Position13078694
GeneNFIX
is asnp
is mentioned by
dbSNPrs398122870
ClinGenrs398122870
ebirs398122870
HLIrs398122870
Exacrs398122870
Varsomers398122870
Maprs398122870
PheGenIrs398122870
hapmaprs398122870
1000 genomesrs398122870
hgdprs398122870
ensemblrs398122870
gopubmedrs398122870
geneviewrs398122870
scholarrs398122870
googlers398122870
pharmgkbrs398122870
gwascentralrs398122870
openSNPrs398122870
23andMers398122870
23andMe allrs398122870
SNP Nexus

SNPshotrs398122870
SNPdbers398122870
MSV3drs398122870
GWAS Ctlgrs398122870
Max Magnitude0
ClinVar
Risk rs398122870(T;T)
Alt rs398122870(T;T)
Reference Rs398122870(;)
Significance Pathogenic
Disease Marshall-Smith syndrome
Variation info
Gene NFIX
CLNDBN Marshall-Smith syndrome
Reversed 0
HGVS NC_000019.9:g.13189508dupT
CLNSRC OMIM Allelic Variant
CLNACC RCV000030638.25,