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rs587779381

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587779381(C;G)
Make rs587779381(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome19
Position13073924
GeneNFIX
is asnp
is mentioned by
dbSNPrs587779381
ebirs587779381
HLIrs587779381
Exacrs587779381
Varsomers587779381
Maprs587779381
PheGenIrs587779381
hapmaprs587779381
1000 genomesrs587779381
hgdprs587779381
ensemblrs587779381
gopubmedrs587779381
geneviewrs587779381
scholarrs587779381
googlers587779381
pharmgkbrs587779381
gwascentralrs587779381
openSNPrs587779381
23andMers587779381
23andMe allrs587779381
SNP Nexus

SNPshotrs587779381
SNPdbers587779381
MSV3drs587779381
GWAS Ctlgrs587779381
Max Magnitude0
ClinVar
Risk rs587779381(G;G)
Alt rs587779381(G;G)
Reference rs587779381(C;C)
Significance Pathogenic
Disease Sotos syndrome 2
Variation info
Gene NFIX
CLNDBN Sotos syndrome 2
Reversed 0
HGVS NC_000019.9:g.13184738C>G
CLNSRC
CLNACC RCV000077780.1,