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rs797045056

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs797045056(-;AGATC)
Make rs797045056(AGATC;AGATC)
ReferenceGRCh38.p2 38.2/147
Chromosome19
Position13025335
GeneNFIX
is asnp
is mentioned by
dbSNPrs797045056
dbSNP (old)rs797045056
ClinGenrs797045056
ebirs797045056
HLIrs797045056
Exacrs797045056
Gnomadrs797045056
Varsomers797045056
Maprs797045056
PheGenIrs797045056
Biobankrs797045056
1000 genomesrs797045056
hgdprs797045056
ensemblrs797045056
gopubmedrs797045056
geneviewrs797045056
scholarrs797045056
googlers797045056
pharmgkbrs797045056
gwascentralrs797045056
openSNPrs797045056
23andMers797045056
23andMe allrs797045056
SNP Nexus

SNPshotrs797045056
SNPdbers797045056
MSV3drs797045056
GWAS Ctlgrs797045056
Max Magnitude0
ClinVar
Risk rs797045056(AGATC;AGATC)
Alt rs797045056(AGATC;AGATC)
Reference Rs797045056(-;-)
Significance Pathogenic
Disease Sotos syndrome 2
Variation info
Gene NFIX
CLNDBN Sotos syndrome 2
Reversed 0
HGVS NC_000019.9:g.13136145_13136149dupAGATC
CLNSRC Baylor College of Medicine
CLNACC RCV000191110.1,