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rs398122876

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs398122876(A;A)
Make rs398122876(A;G)
ReferenceGRCh38 38.1/141
Chromosome19
Position13075672
GeneNFIX
is asnp
is mentioned by
dbSNPrs398122876
ebirs398122876
HLIrs398122876
Exacrs398122876
Varsomers398122876
Maprs398122876
PheGenIrs398122876
hapmaprs398122876
1000 genomesrs398122876
hgdprs398122876
ensemblrs398122876
gopubmedrs398122876
geneviewrs398122876
scholarrs398122876
googlers398122876
pharmgkbrs398122876
gwascentralrs398122876
openSNPrs398122876
23andMers398122876
23andMe allrs398122876
SNP Nexus

SNPshotrs398122876
SNPdbers398122876
MSV3drs398122876
GWAS Ctlgrs398122876
Max Magnitude0
ClinVar
Risk rs398122876(A,T;A,T)
Alt rs398122876(A,T;A,T)
Reference rs398122876(G;G)
Significance Pathogenic
Disease Marshall-Smith syndrome
Variation info
Gene NFIX
CLNDBN Marshall-Smith syndrome
Reversed 0
HGVS NC_000019.9:g.13186486G>A; NC_000019.9:g.13186486G>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000030644.25, RCV000030645.21,