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rs797044939

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs797044939(A;G)
Make rs797044939(G;G)
ReferenceGRCh38.p2 38.2/147
Chromosome19
Position49061477
GeneLOC105376902, NTF4
is asnp
is mentioned by
dbSNPrs797044939
ebirs797044939
HLIrs797044939
Exacrs797044939
Varsomers797044939
Maprs797044939
PheGenIrs797044939
hapmaprs797044939
1000 genomesrs797044939
hgdprs797044939
ensemblrs797044939
gopubmedrs797044939
geneviewrs797044939
scholarrs797044939
googlers797044939
pharmgkbrs797044939
gwascentralrs797044939
openSNPrs797044939
23andMers797044939
23andMe allrs797044939
SNP Nexus

SNPshotrs797044939
SNPdbers797044939
MSV3drs797044939
GWAS Ctlgrs797044939
Max Magnitude0
ClinVar
Risk rs797044939(G;G)
Alt rs797044939(G;G)
Reference rs797044939(A;A)
Significance Probable-Pathogenic
Disease Inborn genetic diseases
Variation info
Gene NTF4
CLNDBN Inborn genetic diseases
Reversed 1
HGVS NC_000019.9:g.49564734T>C
CLNSRC
CLNACC RCV000190785.1,