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rs797044911

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs797044911(C;T)
Make rs797044911(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome19
Position13025354
GeneNFIX
is asnp
is mentioned by
dbSNPrs797044911
ebirs797044911
HLIrs797044911
Exacrs797044911
Varsomers797044911
Maprs797044911
PheGenIrs797044911
hapmaprs797044911
1000 genomesrs797044911
hgdprs797044911
ensemblrs797044911
gopubmedrs797044911
geneviewrs797044911
scholarrs797044911
googlers797044911
pharmgkbrs797044911
gwascentralrs797044911
openSNPrs797044911
23andMers797044911
23andMe allrs797044911
SNP Nexus

SNPshotrs797044911
SNPdbers797044911
MSV3drs797044911
GWAS Ctlgrs797044911
Max Magnitude0
ClinVar
Risk rs797044911(T;T)
Alt rs797044911(T;T)
Reference rs797044911(C;C)
Significance Pathogenic
Disease Inborn genetic diseases
Variation info
Gene NFIX
CLNDBN Inborn genetic diseases
Reversed 0
HGVS NC_000019.9:g.13136168C>T
CLNSRC
CLNACC RCV000190740.1,