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rs387907255

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs387907255(C;C)
Make rs387907255(C;G)
ReferenceGRCh38 38.1/141
Chromosome19
Position13025355
GeneNFIX
is asnp
is mentioned by
dbSNPrs387907255
ebirs387907255
HLIrs387907255
Exacrs387907255
Varsomers387907255
Maprs387907255
PheGenIrs387907255
hapmaprs387907255
1000 genomesrs387907255
hgdprs387907255
ensemblrs387907255
gopubmedrs387907255
geneviewrs387907255
scholarrs387907255
googlers387907255
pharmgkbrs387907255
gwascentralrs387907255
openSNPrs387907255
23andMers387907255
23andMe allrs387907255
SNP Nexus

SNPshotrs387907255
SNPdbers387907255
MSV3drs387907255
GWAS Ctlgrs387907255
Max Magnitude0
ClinVar
Risk rs387907255(C;C)
Alt rs387907255(C;C)
Reference rs387907255(G;G)
Significance Pathogenic
Disease Sotos syndrome 2
Variation info
Gene NFIX
CLNDBN Sotos syndrome 2
Reversed 0
HGVS NC_000019.9:g.13136169G>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000030647.21,